chr15:40695367:G>C Detail (hg38) (RAD51)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr15:40,987,565-40,987,565 View the variant detail on this assembly version.
hg38	chr15:40,695,367-40,695,367

HGVS

RAD51

Type	Transcript	Protein
RefSeq	NM_002875.4:c.-61G>C
	NM_001164269.1:c.-3+46G>C
	NM_001164270.1:c.-61G>C
Ensemble	ENST00000267868.8:c.-61G>C
	ENST00000382643.7:c.-3+46G>C
	ENST00000423169.6:c.-61G>C
	ENST00000557850.5:c.-61G>C
	ENST00000645673.2:c.-61G>C

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star	[No Data.]
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Links

RAD51

Type	Database	ID	Link
Gene	MIM	179617	OMIM
	HGNC	9817	HGNC
	Ensembl	ENSG00000051180	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar	tgv171568761	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

[No Data.]

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
<0.001	Non-small cell lung carcinoma	We genotyped six potentially functional single nucleotide polymorphisms (SNPs) (...	BeFree	21647442	Detail

Annotation

Annotations

Descrption	Source	Links
We genotyped six potentially functional single nucleotide polymorphisms (SNPs) (i.e., RAD51 -135G&gt...	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: rs1801321 dbSNP
Genome: hg38
Position: chr15:40,695,367-40,695,367
Variant Type: snv
Reference Allele: G
Alternative Allele: C

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