Variant #0000892099 (NC_000015.9:g.45695154G>T, NM_001482.2:c.-24503C>A (GATM))

Chromosome 15
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.45695154G>T
DNA change (hg38) -
Published as SPATA5L1(NM_024063.3):c.527G>T (p.(Gly176Val), p.G176V)
ISCN -
DB-ID GATM_009057 See all 3 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) 0.00078 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GATM NM_001482.2 +/. - c.-24503C>A r.(?) p.(=)
SPATA5L1 NM_024063.2 +/. - c.527G>T r.(?) p.(Gly176Val)


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