Variant #0000283818 (NC_000016.9:g.15808755G>A, NC_000016.9(NM_001040113.1):c.5807+11C>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.15808755G>A
DNA change (hg38) g.15714898G>A
Published as MYH11(NM_001040113.2):c.5807+11C>T
ISCN -
DB-ID MYH11_000012
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) 0.0003 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 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.5807+11C>T r.(=) p.(=)
MYH11 NM_002474.2 -?/. - c.5786+11C>T r.(=) p.(=)
NDE1 NM_017668.2 -?/. - c.948-9293G>A r.(=) p.(=)


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