Transcript #00000164

Transcript name transcript variant 2
Gene name LIAS (lipoic acid synthetase)
Chromosome 4
Transcript - NCBI ID NM_194451.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_919433.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

50 entries on 1 page. Showing entries 1 - 50.
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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.643G>A p.(Asp215Asn) - - - -
./. - - c.645T>A p.(Asp215Glu) - - - -
./. - - c.650G>A p.(Arg217Gln) - - - -
./. - - c.657T>A p.(Asp219Glu) - - - -
./. - - c.683T>C p.(Leu228Pro) - - - -
./. - - c.725C>T p.(Pro242Leu) - - - -
./. - - c.726G>A p.(=) - - - -
./. - - c.737+1G>A p.? - - - -
./. - - c.737+9G>A p.(=) - - - -
+/+ - 8/11 c.746G>A p.(=) probably_damaging(1) missense_variant - deleterious(0)
./. - - c.746G>A p.(Arg249His) - - - -
./. - - c.751C>T p.(Pro251Ser) - - - -
./. - - c.797A>G p.(Lys266Arg) - - - -
./. - - c.849C>T p.(=) - - - -
./. - - c.890G>A p.(Arg297His) - - - -
./. - - c.944G>A p.(Arg315His) - - - -
./. - - c.*21_*25del p.(=) - - - -
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