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     
0000001497 +/+ Unknown M subst m.14487T>C - 4.050 - chrM_000034 MSCV_0001497 rs199476109 - ; clinVar; Mitomap; Ensembl; 14520668;14684687;15576045;12205655;14595656 - - - -
0000023339 +/+ Unknown M - m.14487T>C - - - chrM_000034 MSCV_0001497 - - ; clinvar; - - - - -
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