Variant #0000984818 (NC_000023.10:g.69502080G>C, NM_004312.2:c.*464G>C (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.69502080G>C
DNA change (hg38) -
Published as RAB41(NM_001032726.2):c.13G>C (p.(Gly5Arg))
ISCN -
DB-ID ARR3_000045
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) 2.0E-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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RAB41 NM_001032726.2 ?/. - c.13G>C r.(?) p.(Gly5Arg)
ARR3 NM_004312.2 ?/. - c.*464G>C r.(=) p.(=)
PDZD11 NM_016484.4 ?/. - c.*4852C>G r.(=) p.(=)


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