View all genomic variants

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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     
0000004014 ?/? Unknown M subst m.14180T>C - 0.864 - chrM_000548 MSCV_0004014 rs200933339 - ; - - - - -
0000015096 ./. Unknown M - m.14180T>C - - - chrM_000548 MSCV_0004014 - - ; Somatic:ICGC; - - - - Lishuang Shen
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