chr14:69034682:C>T Detail (hg19) (RAD51B)

Information

Genome

Assembly Position
hg19 chr14:69,034,682-69,034,682
hg38 chr14:68,567,965-68,567,965 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_133509.3:c.1037-26520C>T
NM_001321809.1:c.1037-43041C>T
NM_001321810.1:c.1037-43041C>T
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance Benign
Review star
Show details
Links
Type Database ID Link
Gene MIM 602948 OMIM
HGNC 9822 HGNC
Ensembl ENSG00000182185 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Benign 2019-06-14 criteria provided, single submitter not provided germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
<0.001 breast carcinoma We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.132 Malignant neoplasm of breast We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.024 Triple Negative Breast Neoplasms We identified six single-nucleotide polymorphisms, including rs2046210 (ESR1), r... BeFree 21844186 Detail
<0.001 Triple Negative Breast Neoplasms We identified six single-nucleotide polymorphisms, including rs2046210 (ESR1), r... BeFree 21844186 Detail
<0.001 Triple Negative Breast Neoplasms We identified six single-nucleotide polymorphisms, including rs2046210 (ESR1), r... BeFree 21844186 Detail
0.001 breast carcinoma We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.001 Malignant neoplasm of breast We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.003 breast carcinoma We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.123 Malignant neoplasm of breast We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662... BeFree 21791674 Detail
0.121 Malignant neoplasm of breast Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
0.002 breast carcinoma Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
0.003 breast carcinoma Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
<0.001 breast carcinoma Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
0.031 breast carcinoma Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
<0.001 Malignant neoplasm of breast Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
0.230 Malignant neoplasm of breast Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
0.138 Malignant neoplasm of breast Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
0.122 Malignant neoplasm of breast Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
<0.001 breast carcinoma Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
0.009 breast carcinoma Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
0.132 Malignant neoplasm of breast Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall br... BeFree 23593120 Detail
0.132 Malignant neoplasm of breast Large-scale genotyping identifies 41 new loci associated with breast cancer risk... GWASCAT 23535729 Detail
0.132 Malignant neoplasm of breast A multistage genome-wide association study in breast cancer identifies two new r... GWASCAT 19330030 Detail
0.003 breast carcinoma Large-scale genome-wide association studies (GWAS) have been conducted and repor... BeFree 24729084 Detail
0.132 Malignant neoplasm of breast [A multistage genome-wide association study in breast cancer identifies two new ... GAD 19330030 Detail
0.132 Malignant neoplasm of breast Large-scale genome-wide association studies (GWAS) have been conducted and repor... BeFree 24729084 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_133509.5(RAD51B):c.1037-26520C>T AND not provided ClinVar Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We identified six single-nucleotide polymorphisms, including rs2046210 (ESR1), rs12662670 (ESR1), rs... DisGeNET Detail
We identified six single-nucleotide polymorphisms, including rs2046210 (ESR1), rs12662670 (ESR1), rs... DisGeNET Detail
We identified six single-nucleotide polymorphisms, including rs2046210 (ESR1), rs12662670 (ESR1), rs... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
We genotyped 17 germline SNPs (FGFR2-rs2981582, FGFR2-rs3750817, TNRC9-rs3803662, 2q35-rs13387042, M... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Seven SNPs were statistically significant (P ≤ 0.05) with the risk of overall breast cancer in the s... DisGeNET Detail
Large-scale genotyping identifies 41 new loci associated with breast cancer risk. DisGeNET Detail
A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.... DisGeNET Detail
Large-scale genome-wide association studies (GWAS) have been conducted and reported the association ... DisGeNET Detail
[A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11... DisGeNET Detail
Large-scale genome-wide association studies (GWAS) have been conducted and reported the association ... DisGeNET Detail

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs999737 dbSNP
Genome
hg19
Position
chr14:69,034,682-69,034,682
Variant Type
snv
Reference Allele
C
Alternative Allele
T
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