Variant #0000567284 (NC_000019.9:g.39219082_39219090dup, NC_000019.9(NM_004924.4):c.2418+416_2418+424dup (ACTN4))

Chromosome 19
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.39219082_39219090dup
DNA change (hg38) g.38728442_38728450dup
Published as ACTN4(NM_004924.6):c.2418+410_2418+418dupTCCTCCTCC, ACTN4(NM_004924.6):c.2418+413_2418+421dupTCCTCCTCC
ISCN -
DB-ID ACTN4_000026
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ACTN4 NM_004924.4 -/. - c.2418+416_2418+424dup r.(=) p.(=)
CAPN12 NM_144691.3 -/. - c.*2433_*2441dup r.(=) p.(=)


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