All transcript variants in gene SPTLC2

Information The variants shown are described using the NM_004863.3 transcript reference sequence.

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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

dbSNP ID     

Frequency     

Allele Count     

Allele Number     

Combined Depth     

Heterozygote     

Homozygous     

Owner     
./. - c.632-84T>C r.(=) p.(=) g.78036935A>G - SPTLC2_000037 rs4903606 0.502 249 496 1765 - - Admin
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