Variant #0000984819 (NC_000023.10:g.69503184C>T, NM_004312.2:c.*1568C>T (ARR3))

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.69503184C>T
DNA change (hg38) -
Published as RAB41(NM_001363807.1):c.304C>T (p.(Arg102Cys))
ISCN -
DB-ID ARR3_000046
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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB41 NM_001032726.2 ?/. - c.301C>T r.(?) p.(Arg101Cys)
ARR3 NM_004312.2 ?/. - c.*1568C>T r.(=) p.(=)
PDZD11 NM_016484.4 ?/. - c.*3748G>A r.(=) p.(=)


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