Variant #0001034214 (NC_000003.11:g.9834822_9834835dup, NC_000003.11(NM_001198793.1):c.3+14_3+27dup (ARPC4-TTLL3))

Chromosome 3
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.9834822_9834835dup
DNA change (hg38) -
Published as ARPC4(NM_001198780.3):c.17_30dup (p.(Thr11Alafs*23))
ISCN -
DB-ID ARPC4_000004
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARPC4 NM_001024959.2 -?/. - c.-268+433_-268+446dup r.(=) p.(=)
TTLL3 NM_001025930.3 -?/. - c.-16869_-16856dup r.(?) p.(=)
ARPC4-TTLL3 NM_001198793.1 -?/. - c.3+14_3+27dup r.(=) p.(=)


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