Variant #0000951426 (NC_000020.10:g.33593482C>T, NM_020884.3:c.*3491C>T (MYH7B))

Chromosome 20
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.33593482C>T
DNA change (hg38) -
Published as TRPC4AP(NM_015638.3):c.1936+16G>A
ISCN -
DB-ID MYH7B_000122
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) 0.00013 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +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     
TRPC4AP NM_015638.2 -/. - c.1936+16G>A r.(=) p.(=)
MYH7B NM_020884.3 -/. - c.*3491C>T r.(=) p.(=)


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