Genomic variant #0000783607
Individual ID |
00000003 |
Chromosome |
20 |
Allele |
Unknown |
Affects function (reported) |
Not classified |
Affects function (concluded) |
Not classified |
DNA change (genomic) (Relative to hg38 / GRCh38) |
g.25295707G>A |
Reference |
dbSNP |
DB-ID |
PYGB_000103 |
Frequency |
0.439 |
Allele Count |
93 |
Allele Number |
212 |
Depth |
4655 |
Average frequency (large NGS studies) |
Variant not found in online data sets |
Owner |
Admin |
Variant on transcripts
Screenings
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