Variant: 16-48224287-C-T
Transcript: 7
Gene: ABCC11 (ENSG00000121270)
Chromosome: chr16
Position: chr16-48224287
HGVS Consequence: NC_000016.10:g.48224287C>T
VEP Annotation:
Clinical Significance: Benign / likely benign
Number of Homozygous: 17
Annotation Group: Missense / Inframe indel
Clinvar Category: Benign / likely benign
Flags: None
Allele Frequency: 0.174
Allele Number: 1114
Allele Count: 194
Population Allele Frequency
Alternative Transcripts
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