Variant #0000807094 (NC_000016.9:g.15917142C>T, NM_001040113.1:c.472G>A (MYH11))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.15917142C>T
DNA change (hg38) -
Published as MYH11(NM_001040113.1):c.472G>A (p.A158T), MYH11(NM_001040113.2):c.472G>A (p.A158T), MYH11(NM_002474.3):c.472G>A (p.A158T)
ISCN -
DB-ID MYH11_000209 See all 4 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) 0.00012 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH11 NM_001040113.1 -?/. - c.472G>A r.(?) p.(Ala158Thr)
MYH11 NM_002474.2 -?/. - c.472G>A r.(?) p.(Ala158Thr)
NDE1 NM_017668.2 -?/. - c.*99034C>T r.(=) p.(=)


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