chr2:215632255:CA>TG Detail (hg19) (BARD1)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr2:215,632,255-215,632,256 |
hg38 | chr2:214,767,531-214,767,532 View the variant detail on this assembly version. |
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 |
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
Descrption | Source | Links |
---|---|---|
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
- hg19
- Position
- chr2:215,632,255-215,632,256
- Variant Type
- snv
- Reference Allele
- CA
- Alternative Allele
- TG
Genome browser