Variant #0000556869 (NC_000016.9:g.15872688G>A, NM_001040113.1:c.760C>T (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.15872688G>A
DNA change (hg38) g.15778831G>A
Published as MYH11(NM_001040113.1):c.760C>T (p.R254C, p.(Arg254Cys)), MYH11(NM_001040113.2):c.760C>T (p.R254C)
ISCN -
DB-ID MYH11_000116 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) 0.00177 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH11 NM_001040113.1 -?/. - c.760C>T r.(?) p.(Arg254Cys)
MYH11 NM_002474.2 -?/. - c.739C>T r.(?) p.(Arg247Cys)
NDE1 NM_017668.2 -?/. - c.*54580G>A r.(=) p.(=)


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