All transcript variants in gene DCAF12L2

Information The variants shown are described using the NM_001013628.2 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.811A>G r.(?) p.(Ser271Gly) - likely benign g.125299097T>C - DCAF12L2(NM_001013628.2):c.811A>G (p.S271G) - DCAF12L2_000008 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Rotterdam
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