Variant #0000503552 (NC_000001.10:g.155205634T>C, NM_000157.3:c.1226A>G (GBA))

Chromosome 1
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.155205634T>C
DNA change (hg38) g.155235843T>C
Published as GBA(NM_000157.3):c.1226A>G (p.(Asn409Ser)), GBA(NM_000157.4):c.1226A>G (p.N409S), GBA1(NM_001005741.3):c.1226A>G (p.N409S)
ISCN -
DB-ID GBA_000005 See all 119 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) 0.00232 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 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GBA NM_000157.3 +/. - c.1226A>G r.(?) p.(Asn409Ser)


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