Variant #0000577136 (NC_000023.10:g.69503438T>C, ARR3(NM_004312.2):c.*1822T>C)

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.69503438T>C
DNA change (hg38) g.70283588T>C
Published as RAB41(NM_001032726.2):c.416T>C (p.M139T)
ISCN -
DB-ID ARR3_000028
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
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.416T>C r.(?) p.(Met139Thr)
ARR3 NM_004312.2 ?/. - c.*1822T>C r.(=) p.(=)
PDZD11 NM_016484.4 ?/. - c.*3494A>G r.(=) p.(=)