Variant #0001037626 (NC_000009.11:g.94794767C>A, NM_006415.2:c.1402G>T (SPTLC1))

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.94794767C>A
DNA change (hg38) -
Published as SPTLC1(NM_001368273.1):c.937G>T (p.A313S), SPTLC1(NM_006415.4):c.1402G>T (p.(Ala468Ser))
ISCN -
DB-ID SPTLC1_000053 See all 2 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) 9.0E-5 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTLC1 NM_006415.2 -?/. - c.1402G>T r.(?) p.(Ala468Ser)


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