Variant #0000308818 (NC_000014.8:g.77978652G>A, NM_004863.3:c.1664C>T (SPTLC2))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.77978652G>A
DNA change (hg38) g.77512309G>A
Published as SPTLC2(NM_004863.3):c.1664C>T (p.T555M), SPTLC2(NM_004863.4):c.1664C>T (p.T555M)
ISCN -
DB-ID SPTLC2_000017 See all 4 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) 0.00504 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
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     
SPTLC2 NM_004863.3 -/. - c.1664C>T r.(?) p.(Thr555Met)


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