Chr Mutation (hg38) CAid Gene Transcript Linkouts
13g.40799096C>GCA340495SLC25A15,TPTE2P5c.95C>G (p.Thr32Arg)
n.416C>G
n.2251G>C
n.2080G>C
 ClinVar dbSNP
13g.40799096C>TCA6959624SLC25A15,TPTE2P5c.95C>T (p.Thr32Ile)
n.416C>T
n.2251G>A
n.2080G>A
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched