All variants in the MYLK2 gene

Information The variants shown are described using the NM_033118.3 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.1204G>T r.(?) p.(Val402Phe) - likely benign g.30414721G>T g.31826918G>T - - MYLK2_000057 1 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs779637525 Germline - 1/2795 individuals - 0 - Mohammed Faruq
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