Variant #0000725473 (NC_000016.9:g.15872264T>C, NC_000016.9(NM_001040113.1):c.811+373A>G (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.15872264T>C
DNA change (hg38) -
Published as MYH11(NM_001040113.2):c.811+373A>G
ISCN -
DB-ID MYH11_000274
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 2021-02-08 18:36:18 +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.811+373A>G r.(=) p.(=)
MYH11 NM_002474.2 -?/. - c.790+373A>G r.(=) p.(=)
NDE1 NM_017668.2 -?/. - c.*54156T>C r.(=) p.(=)


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