Variant #0000306705 (NC_000023.10:g.69503221C>T, ARR3(NM_004312.2):c.*1605C>T)

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.69503221C>T
DNA change (hg38) g.70283371C>T
Published as RAB41(NM_001032726.2):c.338C>T (p.T113I, p.(Thr113Ile))
ISCN -
DB-ID RAB41_000014 See all 2 reported entries
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) 7.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2019-12-04 15:24:38 +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.338C>T r.(?) p.(Thr113Ile)
ARR3 NM_004312.2 -/. - c.*1605C>T r.(=) p.(=)
PDZD11 NM_016484.4 -/. - c.*3711G>A r.(=) p.(=)