Unique variants in gene MYNN

Information The variants shown are described using the NM_018657.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

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     
-?/. 1 - c.1676A>G likely benign r.(?) p.(Asp559Gly) g.169504309A>G - MYNN(NM_001185118.1):c.1676A>G (p.(Asp559Gly), p.(Asp530Gly)) - MYNN_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
-?/. 1 - c.*7008G>C likely benign r.(=) p.(=) g.169511474G>C - LRRC34(NM_001172779.1):c.1344C>G (p.(Asp448Glu), p.(=), p.(Asp416Glu)) - MYNN_000002 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL
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