Variant #0000912004 (NC_000003.11:g.9868869C>T, NM_001198793.1:c.1246C>T (ARPC4-TTLL3))

Chromosome 3
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.9868869C>T
DNA change (hg38) -
Published as TTLL3(NM_001025930.5):c.1492C>T (p.R498C)
ISCN -
DB-ID ARPC4_000002
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) 0.00059 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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.*20970C>T r.(=) p.(=)
TTLL3 NM_001025930.3 ?/. - c.1492C>T r.(?) p.(Arg498Cys)
ARPC4-TTLL3 NM_001198793.1 ?/. - c.1246C>T r.(?) p.(Arg416Cys)


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