Variant #0000981623 (NC_000016.9:g.15802694dup, NM_001040113.1:c.5819dup (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.15802694dup
DNA change (hg38) -
Published as MYH11(NM_002474.3):c.5787-4707dupC
ISCN -
DB-ID MYH11_000341
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MYH11 NM_001040113.1 -?/. - c.5819dup r.(?) p.(Gln1941Thrfs*20)
MYH11 NM_002474.2 -?/. - c.5787-4707dup r.(=) p.(=)
NDE1 NM_017668.2 -?/. - c.947+11977dup r.(=) p.(=)


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