Variant #0000728805 (NC_000023.10:g.2871204C>G, NM_000047.2:c.410G>C (ARSE))

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.2871204C>G
DNA change (hg38) -
Published as ARSE(NM_000047.2):c.410G>C (p.(Gly137Ala)), ARSE(NM_001282628.1):c.485G>C (p.G162A), ARSL(NM_000047.3):c.410G>C (p.G137A)
ISCN -
DB-ID ARSE_000007 See all 10 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) 0.00013 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
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     
ARSE NM_000047.2 +/. - c.410G>C r.(?) p.(Gly137Ala)


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