Variant #0000914473 (NC_000016.9:g.15809105C>T, NM_001040113.1:c.5550G>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.15809105C>T
DNA change (hg38) -
Published as MYH11(NM_001040113.1):c.5550G>A (p.S1850=), MYH11(NM_001040113.2):c.5550G>A (p.S1850=)
ISCN -
DB-ID MYH11_000264 See all 3 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) 0.00053 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 2023-01-11 15:44:22 +01:00 (CET)
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.5550G>A r.(?) p.(Ser1850=)
MYH11 NM_002474.2 -?/. - c.5529G>A r.(?) p.(Ser1843=)
NDE1 NM_017668.2 -?/. - c.948-8943C>T r.(=) p.(=)


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