Variant: 17-43042868-T-C
Transcript: 10
Gene: BRCA1 (ENSG00000012048)
Chromosome: chr17
Position: chr17-43042868
HGVS Consequence: NC_000017.11:g.43042868T>C
VEP Annotation:
Clinical Significance: Benign / likely benign
Number of Homozygous: 92
Annotation Group: Other
Clinvar Category: Benign / likely benign
Flags: None
Allele Frequency: 0.405
Allele Number: 1114
Allele Count: 451
Population Allele Frequency
Alternative Transcripts
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