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     
0000001435 +/+ Unknown M subst m.8529G>A - 5.070 - chrM_000052 MSCV_0001435 rs267606881 - ; clinVar; Mitomap; Ensembl; 17954552 - - - -
0000023176 +/+ Unknown M - m.8529G>A - - - chrM_000052 MSCV_0001435 - - ; clinvar; - - - - -
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