chr2:214767531:CA>TG Detail (hg38) (BARD1)

Information

Genome

Assembly Position
hg19 chr2:215,632,255-215,632,256 View the variant detail on this assembly version.
hg38 chr2:214,767,531-214,767,532

HGVS

Type Transcript Protein
RefSeq NM_000465.3:c.1518_1519delinsCA NP_000456.2:p.Val507Met
NR_104212.1:c.1518_1519delinsCA
NR_104216.1:c.1518_1519delinsCA
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 601593 OMIM
HGNC 952 HGNC
Ensembl ENSG00000138376 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
[No Data.]
CIViC
[No Data.]
DisGeNET
Score Disease name Description Source Pubmed Links
0.008 breast carcinoma Genetic polymorphism of BARD1 (Val/Met 507) could be useful in the selection of ... BeFree 14550946 Detail
0.008 breast carcinoma BARD1 variants Cys557Ser and Val507Met in breast cancer predisposition. BeFree 16333312 Detail
0.121 Breast Cancer, Familial These results suggest that the contribution of the BARD1 germline variants to br... BeFree 16333312 Detail
0.114 Malignant neoplasm of breast BARD1 variants Cys557Ser and Val507Met in breast cancer predisposition. BeFree 16333312 Detail
0.114 Malignant neoplasm of breast Genetic polymorphism of BARD1 (Val/Met 507) could be useful in the selection of ... BeFree 14550946 Detail
Annotation

Annotations

DescrptionSourceLinks
Genetic polymorphism of BARD1 (Val/Met 507) could be useful in the selection of postmenopausal women... DisGeNET Detail
BARD1 variants Cys557Ser and Val507Met in breast cancer predisposition. DisGeNET Detail
These results suggest that the contribution of the BARD1 germline variants to breast cancer predispo... DisGeNET Detail
BARD1 variants Cys557Ser and Val507Met in breast cancer predisposition. DisGeNET Detail
Genetic polymorphism of BARD1 (Val/Met 507) could be useful in the selection of postmenopausal women... 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
rs386654966 dbSNP
Genome
hg38
Position
chr2:214,767,531-214,767,532
Variant Type
snv
Reference Allele
CA
Alternative Allele
TG
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