Variant #0001065040 (NC_000009.11:g.4574003dup, NM_004170.5:c.864dup (SLC1A1))

Chromosome 9
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.4574003dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID PPAPDC2_000007
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPATA6L NM_001039395.3 ?/. - c.*26808dup r.(?) p.(=)
SLC1A1 NM_004170.5 ?/. - c.864dup r.(?) p.(Val289Serfs*57)
PPAPDC2 NM_203453.3 ?/. - c.-88373dup r.(?) p.(=)


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