Variant #0000575475 (NC_000023.10:g.2867554_2867574dup, NM_000047.2:c.632_652dup (ARSE))

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.2867554_2867574dup
DNA change (hg38) g.2949513_2949533dup
Published as ARSL(NM_001282628.2):c.707_727dupTGGTAGCAGGGAAGCTCACAC (p.L236_T242dup)
ISCN -
DB-ID ARSE_000085
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSE NM_000047.2 ?/. - c.632_652dup r.(?) p.(Leu211_Thr217dup)


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