Variant #0001040388 (NC_000015.9:g.45695366A>T, NM_001482.2:c.-24715T>A (GATM))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.45695366A>T
DNA change (hg38) -
Published as SPATA5L1(NM_024063.3):c.739A>T (p.(Lys247*))
ISCN -
DB-ID GATM_009063
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GATM NM_001482.2 ?/. - c.-24715T>A r.(?) p.(=)
SPATA5L1 NM_024063.2 ?/. - c.739A>T r.(?) p.(Lys247*)


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