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     
0000001436 +?/+? Unknown M ins m.8617_8618insT - - - chrM_000053 MSCV_0001436 rs387906423 - ; clinVar; 19124644 - - - -
0000023181 -?/-? Unknown M - m.8617_8618insT - - - chrM_000053 MSCV_0001436 - - ; clinvar; - - - - -
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