Variant #0001040812 (NC_000016.9:g.15809117C>T, NM_001040113.1:c.5538G>A (MYH11))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.15809117C>T
DNA change (hg38) -
Published as MYH11(NM_001040113.2):c.5538G>A (p.A1846=), MYH11(NM_002474.3):c.5517G>A (p.(Ala1839=))
ISCN -
DB-ID MYH11_000018 See all 2 reported entries
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) 0.03417 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.5538G>A r.(?) p.(Ala1846=)
MYH11 NM_002474.2 -/. - c.5517G>A r.(?) p.(Ala1839=)
NDE1 NM_017668.2 -/. - c.948-8931C>T r.(=) p.(=)


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