Variant #0000556722 (NC_000016.9:g.15797967T>A, NM_001040113.1:c.*22A>T (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.15797967T>A
DNA change (hg38) g.15704110T>A
Published as MYH11(NM_001040113.1):c.*22A>T (p.(=)), MYH11(NM_001040114.1):c.5821A>T (p.T1941S), MYH11(NM_002474.3):c.5800A>T (p.T1934S)
ISCN -
DB-ID MYH11_000006 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) 0.00137 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +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.*22A>T r.(=) p.(=)
MYH11 NM_002474.2 ?/. - c.5800A>T r.(?) p.(Thr1934Ser)
NDE1 NM_017668.2 ?/. - c.947+7250T>A r.(=) p.(=)


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