chr16:14043175:C>G Detail (hg19) (ERCC4)

Information

Genome

Assembly Position
hg19 chr16:14,043,175-14,043,175
hg38 chr16:13,949,318-13,949,318 View the variant detail on this assembly version.

HGVS

Type Transcript Protein
RefSeq NM_005236.2:c.*971C>G
Ensemble ENST00000311895.8:c.*971C>G
ENST00000682617.1:c.*971C>G
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

JP HGVD:[No Data.]
ToMMo:0.238
NCBN:[No Data.]
NCBN(Hondo):[No Data.]
NCBN(Ryukyu):[No Data.]
East asia ExAC:[No Data.]

Prediction

ClinVar

Clinical Significance Benign
Review star
Show details
Links
Type Database ID Link
Gene MIM 133520 OMIM
HGNC 3436 HGNC
Ensembl ENSG00000175595 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar tgv54823840 TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance Last evaluated Review status Condition Origin Links
Benign 2018-01-13 criteria provided, single submitter Xeroderma pigmentosum, group F germline Detail
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.003 Xeroderma pigmentosum, group F We investigated the association between polymorphisms in excision repair cross-c... BeFree 24861646 Detail
0.006 colorectal cancer We investigated the association between polymorphisms in excision repair cross-c... BeFree 24861646 Detail
<0.001 colorectal carcinoma We investigated the association between polymorphisms in excision repair cross-c... BeFree 24861646 Detail
0.444 Xeroderma pigmentosum, group F We investigated the association between polymorphisms in excision repair cross-c... BeFree 24861646 Detail
Annotation

Annotations

DescrptionSourceLinks
NM_005236.3(ERCC4):c.*971C>G AND Xeroderma pigmentosum, group F ClinVar Detail
We investigated the association between polymorphisms in excision repair cross-complementation group... DisGeNET Detail
We investigated the association between polymorphisms in excision repair cross-complementation group... DisGeNET Detail
We investigated the association between polymorphisms in excision repair cross-complementation group... DisGeNET Detail
We investigated the association between polymorphisms in excision repair cross-complementation group... DisGeNET Detail

Overlapped Transcript Coordinates

Gene Transcript ID Exon Number Chromosome Start Stop Type Amino Mutation Transcript Position Links

Overlapped Transcript

Gene Transcript ID Chromosome Start Stop Links
Gene
-
dbSNP
rs2276466 dbSNP
Genome
hg19
Position
chr16:14,043,175-14,043,175
Variant Type
snv
Reference Allele
C
Alternative Allele
G
ToMMo VCF FILTER column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
PASS
Total VCF ID column value (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
rs2276466
Allele frequency, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
0.2377
Allele count in genotypes, for each ALT allele (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
3984
Total number of alleles in called genotypes (ToMMo 8.3KJPN Allele Frequency Panel(v20200831))
16760
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