Variant #0000981641 (NC_000016.9:g.15917118G>T, NM_001040113.1:c.496C>A (MYH11))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.15917118G>T
DNA change (hg38) -
Published as MYH11(NM_002474.3):c.496C>A (p.(Leu166Ile))
ISCN -
DB-ID MYH11_000350
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH11 NM_001040113.1 ?/. - c.496C>A r.(?) p.(Leu166Ile)
MYH11 NM_002474.2 ?/. - c.496C>A r.(?) p.(Leu166Ile)
NDE1 NM_017668.2 ?/. - c.*99010G>T r.(=) p.(=)


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