Variant #0000254013 (NC_000009.11:g.135202325A>C, NM_015046.5:c.4660T>G (SETX))

Chromosome 9
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.135202325A>C
DNA change (hg38) g.132326938A>C
Published as SETX(NM_001351527.2):c.4660T>G (p.C1554G), SETX(NM_015046.5):c.4660T>G (p.C1554G, p.(Cys1554Gly)), SETX(NM_015046.7):c.4660T>G (p.C1554G)
ISCN -
DB-ID SETX_000034 See all 8 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) 0.00555 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SETX NM_015046.5 -?/. - c.4660T>G r.(?) p.(Cys1554Gly)


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