Variant #0000526077 (NC_000005.9:g.78135241C>T, NM_000046.3:c.1151G>A (ARSB))

Chromosome 5
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.78135241C>T
DNA change (hg38) g.78839418C>T
Published as ARSB(NM_000046.4):c.1151G>A (p.S384N), ARSB(NM_000046.5):c.1151G>A (p.S384N)
ISCN -
DB-ID ARSB_000001 See all 11 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) 0.04282 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSB NM_000046.3 -/. - c.1151G>A r.(?) p.(Ser384Asn)


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