Variant #0000896332 (NC_000023.10:g.69498434del, NM_004312.2:c.848del (ARR3))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.69498434del
DNA change (hg38) -
Published as ARR3(NM_004312.2):c.848delG (p.G283Afs*42), ARR3(NM_004312.3):c.848delG (p.G283Afs*42)
ISCN -
DB-ID ARR3_000030 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.-3634del r.(?) p.(=)
ARR3 NM_004312.2 +/. - c.848del r.(?) p.(Gly283AlafsTer42)


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