Variant #0000334523 (NC_000023.10:g.69503181A>T, ARR3(NM_004312.2):c.*1565A>T)

Chromosome X
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.69503181A>T
DNA change (hg38) g.70283331A>T
Published as RAB41(NM_001032726.2):c.298A>T (p.(Ile100Phe))
ISCN -
DB-ID RAB41_000013
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) 6.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB41 NM_001032726.2 ?/. - c.298A>T r.(?) p.(Ile100Phe)
ARR3 NM_004312.2 ?/. - c.*1565A>T r.(=) p.(=)
PDZD11 NM_016484.4 ?/. - c.*3751T>A r.(=) p.(=)