View all genomic variants

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

Effect     

Allele     

Chr     

Type     

AscendingDNA change (genomic) (hg19)     

Published as     

GERP     

Segregation     

DB-ID     

MSCV     

dbSNP ID     

Frequency     

Sources     

Reference     

Variant remarks     

Genetic origin     

Variant_disease     

Owner     
0000004968 ?/? Unknown M subst m.9123G>A - -9.800 - chrM_001232 MSCV_0004968 rs28358270 - ; - - - - -
0000013690 ./. Unknown M - m.9123G>A - - - chrM_001232 MSCV_0004968 - - ; Somatic:COSMIC; - - - - -
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