View all transcript variants in gene C19orf12

Information The variants shown are described using the NM_031448.4 transcript reference sequence.

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Effect     

Location     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     

Chr     

Allele     

Type     

DNA change (genomic) (hg19)     

Published as     

GERP     

Segregation     

DB-ID     

MSCV     

dbSNP ID     

Frequency     

Sources     

Reference     

Variant remarks     

Genetic origin     

Variant_disease     

Owner     
./. - - c.*1592A>G - r.(=) p.(=) - - - - 19 Unknown - g.30192027T>C - - - C19orf12_000078 MSCV_0018655 - - ; clinvar; - - - - -
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