Variant #0000567278 (NC_000019.9:g.39207939G>A, NM_004924.4:c.1126G>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.39207939G>A
DNA change (hg38) g.38717299G>A
Published as ACTN4(NM_004924.4):c.1126G>A (p.(Glu376Lys))
ISCN -
DB-ID ACTN4_000022
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_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.1126G>A r.(?) p.(Glu376Lys)
CAPN12 NM_144691.3 ?/. - c.*13553C>T r.(=) p.(=)


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