Variant #0000567279 (NC_000019.9:g.39208718C>T, NC_000019.9(NM_004924.4):c.1291+4C>T (ACTN4))

Chromosome 19
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.39208718C>T
DNA change (hg38) g.38718078C>T
Published as ACTN4(NM_004924.5):c.1291+4C>T
ISCN -
DB-ID ACTN4_000023
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) 0.00023 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-15 18:00:31 +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.1291+4C>T r.spl? p.?
CAPN12 NM_144691.3 -?/. - c.*12774G>A r.(=) p.(=)


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