Variant #0000556731 (NC_000016.9:g.15808776T>C, NM_001040113.1:c.5797A>G (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.15808776T>C
DNA change (hg38) g.15714919T>C
Published as MYH11(NM_001040113.2):c.5797A>G (p.S1933G)
ISCN -
DB-ID MYH11_000143 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 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.5797A>G r.(?) p.(Ser1933Gly)
MYH11 NM_002474.2 ?/. - c.5776A>G r.(?) p.(Ser1926Gly)
NDE1 NM_017668.2 ?/. - c.948-9272T>C r.(=) p.(=)


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