Variant #0000968108 (NC_000016.9:g.15810812A>G, NC_000016.9(NM_001040113.1):c.5525+185T>C (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.15810812A>G
DNA change (hg38) -
Published as MYH11(NM_002474.3):c.5504+185T>C
ISCN -
DB-ID MYH11_000327
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 2024-02-26 20:06:56 +01:00 (CET)
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.5525+185T>C r.(=) p.(=)
MYH11 NM_002474.2 -?/. - c.5504+185T>C r.(=) p.(=)
NDE1 NM_017668.2 -?/. - c.948-7236A>G r.(=) p.(=)


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