Variant #0000886027 (NC_000003.11:g.9845668C>T, NC_000003.11(NM_001198793.1):c.330+2228C>T (ARPC4-TTLL3))

Chromosome 3
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.9845668C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ARPC4_000001
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:01:21 +01:00 (CET)
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.202C>T r.(?) p.(Arg68Cys)
TTLL3 NM_001025930.3 +?/. - c.-6023C>T r.(?) p.(=)
ARPC4-TTLL3 NM_001198793.1 +?/. - c.330+2228C>T r.(=) p.(=)


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