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.1613C>T r.(?) p.(Pro538Leu) - VUS g.30419842C>T g.31832039C>T MYLK2(NM_033118.3):c.1613C>T (p.P538L) - MYLK2_000035 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Groningen
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