Variant #0000006670 (NC_000014.8:g.78045373C>T, SPTLC2(NM_004863.3):c.407G>A)

Individual ID 00006676
Chromosome 14
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.78045373C>T
Reference Chunyu Li, et al. (2023)
DB-ID SPTLC2_000015
Frequency -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner XY Liu
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by XY Liu
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Variant/VariO/DNA     

Variant/VariO/protein     
SPTLC2 NM_004863.3 ?/. 3 c.407G>A r.(?) p.(Arg136Gln) - -



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000006700 ? ? - 1 XY Liu