Variant #0000283819 (NC_000016.9:g.15802687G>T, NM_001040113.1:c.5819C>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.15802687G>T
DNA change (hg38) g.15708830G>T
Published as MYH11(NM_001040113.1):c.5819C>A (p.P1940Q, p.(Pro1940Gln)), MYH11(NM_001040113.2):c.5819C>A (p.P1940Q)
ISCN -
DB-ID MYH11_000007 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) 0.00127 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 2018-01-15 20:58:59 +01:00 (CET)
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.5819C>A r.(?) p.(Pro1940Gln)
MYH11 NM_002474.2 -?/. - c.5787-4707C>A r.(=) p.(=)
NDE1 NM_017668.2 -?/. - c.947+11970G>T r.(=) p.(=)


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