Variant #0000556720 (NC_000016.9:g.15781283C>T, NM_001040113.1:c.*16706G>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.15781283C>T
DNA change (hg38) g.15687426C>T
Published as NDE1(NM_001143979.1):c.438C>T (p.I146=)
ISCN -
DB-ID MYH11_000138
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.*16706G>A r.(=) p.(=)
MYH11 NM_002474.2 -?/. - c.*16565G>A r.(=) p.(=)
NDE1 NM_017668.2 -?/. - c.438C>T r.(?) p.(Ile146=)


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