Variant #0000976854 (NC_000005.9:g.78181612G>C, NM_000046.3:c.937C>G (ARSB))

Chromosome 5
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.78181612G>C
DNA change (hg38) -
Published as ARSB(NM_000046.4):c.937C>G (p.P313A), ARSB(NM_000046.5):c.937C>G (p.(Pro313Ala))
ISCN -
DB-ID ARSB_000014 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) 0 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 N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSB NM_000046.3 +/. - c.937C>G r.(?) p.(Pro313Ala)


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