Transcript #00000165

Transcript name transcript variant 3
Gene name LIAS (lipoic acid synthetase)
Chromosome 4
Transcript - NCBI ID NM_001278590.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001265519.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

50 entries on 1 page. Showing entries 1 - 50.
Legend  

Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.7C>T p.(=) - - - -
./. - - c.29G>A p.(Arg10His) - - - -
./. - - c.31A>T p.(Thr11Ser) - - - -
./. - - c.35T>A p.(Leu12Gln) - - - -
./. - - c.37G>A p.(Gly13Arg) - - - -
./. - - c.57A>C p.(Arg19Ser) - - - -
./. - - c.59_60insT p.(Cys22Leufs*13) - - - -
./. - - c.60T>C p.(=) - - - -
./. - - c.80C>T p.(Pro27Leu) - - - -
./. - - c.110A>T p.(Glu37Val) - - - -
./. - - c.114C>A p.(=) - - - -
./. - - c.120G>T p.(Gln40His) - - - -
./. - - c.122A>G p.(Asn41Ser) - - - -
./. - - c.129A>G p.(=) - - - -
./. - - c.140A>G p.(Asp47Gly) - - - -
./. - - c.173C>T p.(Thr58Ile) - - - -
./. - - c.218G>C p.(Arg73Thr) - - - -
./. - - c.244A>G p.(Thr82Ala) - - - -
./. - - c.292C>T p.(Arg98Trp) - - - -
./. - - c.306C>A p.(=) - - - -
./. - - c.331T>A p.(Cys111Ser) - - - -
./. - - c.363del p.(Glu122Asnfs*11) - - - -
./. - - c.393+4G>A p.? - - - -
./. - - c.393+8C>A p.(=) - - - -
./. - - c.393+10G>A p.(=) - - - -
./. - - c.403G>C p.(Asp135His) - - - -
./. - - c.473G>C p.(Ser158Thr) - - - -
./. - - c.475_477delinsAAA p.(Glu159Lys) - - - -
./. - - c.529C>T p.(=) - - - -
./. - - c.550+4A>G p.? - - - -
./. - - c.551-1_558del p.? - - - -
./. - - c.563G>C p.(Gly188Ala) - - - -
./. - - c.592T>A p.(Ser198Thr) - - - -
./. - - c.608+2210G>A p.(=) - - - -
./. - - c.608+2212T>A p.(=) - - - -
./. - - c.608+2217G>A p.(=) - - - -
./. - - c.608+2224T>A p.(=) - - - -
./. - - c.608+2250T>C p.(=) - - - -
./. - - c.608+2292C>T p.(=) - - - -
./. - - c.608+2293G>A p.(=) - - - -
./. - - c.608+2305G>A p.(=) - - - -
./. - - c.608+2313G>A p.(=) - - - -
./. - - c.617G>A p.(Arg206His) - - - -
+/+ - 7/10 c.617G>A p.(Arg206His) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.622C>T p.(Pro208Ser) - - - -
./. - - c.668A>G p.(Lys223Arg) - - - -
./. - - c.720C>T p.(=) - - - -
./. - - c.761G>A p.(Arg254His) - - - -
./. - - c.815G>A p.(Arg272His) - - - -
./. - - c.973_977del p.(Thr326Argfs*16) - - - -
Legend