Variant #0000567286 (NC_000019.9:g.39229110G>A, NM_004924.4:c.*9038G>A (ACTN4))

Chromosome 19
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.39229110G>A
DNA change (hg38) g.38738470G>A
Published as CAPN12(NM_144691.3):c.838C>T (p.(Arg280Trp))
ISCN -
DB-ID ACTN4_000028
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) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACTN4 NM_004924.4 ?/. - c.*9038G>A r.(=) p.(=)
CAPN12 NM_144691.3 ?/. - c.838C>T r.(?) p.(Arg280Trp)


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