Variant: 10-97465981-T-A
Transcript: 14
Gene: MMS19 (ENSG00000155229)
Chromosome: chr10
Position: chr10-97465981
HGVS Consequence: NC_000010.11:g.97465981T>A
VEP Annotation:
Clinical Significance: -
Number of Homozygous: 130
Annotation Group: Regulatory
Clinvar Category: -
Flags: None
Allele Frequency: 0.476
Allele Number: 1112
Allele Count: 529
Population Allele Frequency
Alternative Transcripts
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