All genomic variants

2 entries on 1 page. Showing entries 1 - 2.
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Variant ID     

Effect     

Chr     

Classification method     

Clinical classification     

AscendingDNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
0000003406 ?/. 1 - - g.22656863T>G g.22330370T>G - - chr1_000017 - - - - Germline - - - - - Yu Sun
0000011379 ?/. 1 - - g.22656863T>G g.22330370T>G - - chr1_000017 - - - - Germline - - - - - Yu Sun
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