Transcript #00000057

Transcript name transcript variant 2
Gene name C10orf2 (chromosome 10 open reading frame 2)
Chromosome 10
Transcript - NCBI ID NM_001163812.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001157284.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

101 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-650A>G p.(=) - - - -
./. - - c.-644A>T p.(=) - - - -
./. - - c.-605G>T p.(=) - - - -
./. - - c.-585T>G p.(=) - - - -
./. - - c.-549G>A p.(=) - - - -
./. - - c.-470G>A p.(=) - - - -
./. - - c.-423C>T p.(=) - - - -
./. - - c.-307_-306del p.(=) - - - -
./. - - c.-290G>C p.(=) - - - -
./. - - c.-241C>T p.(=) - - - -
./. - - c.-105T>C p.(=) - - - -
./. - - c.76G>A p.(Gly26Ser) - - - -
./. - - c.77G>T p.(Gly26Val) - - - -
+?/+? - 1/5 c.247C>T p.(Pro83Ser) possibly_damaging(0.772) missense_variant - deleterious(0.04)
./. - - c.247C>T p.(Pro83Ser) - - - -
./. - - c.274G>A p.(Gly92Ser) - - - -
./. - - c.276C>T p.(=) - - - -
./. - - c.331del p.(Leu112Serfs*3) - - - -
./. - - c.384C>T p.(=) - - - -
./. - - c.492C>T p.(=) - - - -
./. - - c.639C>T p.(=) - - - -
./. - - c.904C>T p.(Arg302Trp) - - - -
./. - - c.908G>A p.(Arg303Gln) - - - -
+/+ - 1/5 c.908G>A p.(Arg303Gln) possibly_damaging(0.684) missense_variant - deleterious(0.02)
./. - - c.922T>C p.(=) - - - -
+/+ - 1/5 c.944G>A p.(Trp315*) - stop_gained - -
./. - - c.944G>T p.(Trp315Leu) - - - -
./. - 1/5 c.944G>T p.(Trp315Leu) benign(0.167) missense_variant - deleterious(0.01)
./. - - c.952G>A p.(Ala318Thr) - - - -
+/+ - 1/5 c.952G>A p.(Ala318Thr) possibly_damaging(0.877) missense_variant - deleterious(0.01)
+/+ - 1/5 c.955A>C p.(Lys319Gln) possibly_damaging(0.823) missense_variant - deleterious(0.01)
./. - - c.955A>G p.(Lys319Glu) - - - -
+/+ - 1/5 c.955A>G p.(Lys319Glu) possibly_damaging(0.864) missense_variant - deleterious(0.01)
+/+ - 1/5 c.1001G>A p.(Arg334Gln) benign(0.158) missense_variant - tolerated(0.06)
./. - - c.1001G>A p.(Arg334Gln) - - - -
./. - - c.1003C>A p.(Pro335Thr) - - - -
./. - - c.1042G>A p.(Gly348Arg) - - - -
./. - - c.1052A>G p.(Asn351Ser) - - - -
./. - - c.1061G>C p.(Arg354Pro) - - - -
+/+ - 1/5 c.1061G>C p.(Arg354Pro) benign(0.016) missense_variant - tolerated(0.23)
./. - - c.1070G>C p.(Arg357Pro) - - - -
./. - - c.1075G>A p.(Ala359Thr) - - - -
+/+ - 1/5 c.1075G>A p.(Ala359Thr) possibly_damaging(0.907) missense_variant - deleterious(0.01)
./. - 1/5 c.1075G>T p.(Ala359Ser) possibly_damaging(0.54) missense_variant - tolerated(0.19)
./. - - c.1101C>T p.(=) - - - -
./. - - c.1102G>A p.(Val368Ile) - - - -
./. - - c.1106C>A p.(Ser369Tyr) - - - -
+/+ - 1/5 c.1106C>A p.(Ser369Tyr) possibly_damaging(0.642) missense_variant - deleterious(0)
./. - 1/5 c.1106C>T p.(Ser369Phe) possibly_damaging(0.898) missense_variant - deleterious(0)
./. - - c.1120C>T p.(Arg374Trp) - - - -
+/+ - 1/5 c.1120C>T p.(Arg374Trp) benign(0.327) missense_variant - deleterious(0)
./. - - c.1121G>A p.(Arg374Gln) - - - -
+/+ - 1/5 c.1142T>C p.(Leu381Pro) benign(0.236) missense_variant - deleterious(0.03)
./. - - c.1142T>C p.(Leu381Pro) - - - -
./. - 1/5 c.1142T>G p.(Leu381Arg) probably_damaging(0.954) missense_variant - deleterious(0)
./. - - c.1172G>A p.(Arg391His) - - - -
./. - - c.1196A>G p.(Asn399Ser) - - - -
./. - - c.1287C>T p.(=) - - - -
+/+ - 2/5 c.1287C>T p.(=) - synonymous_variant - -
+?/+? - 2/5 c.1366C>G p.(Leu456Val) possibly_damaging(0.739) missense_variant - deleterious(0)
./. - - c.1366C>G p.(Leu456Val) - - - -
./. - - c.1370C>T p.(Thr457Ile) - - - -
+/+ - 2/5 c.1370C>T p.(Thr457Ile) possibly_damaging(0.703) missense_variant - deleterious(0.04)
./. - - c.1374G>T p.(Gln458His) - - - -
./. - - c.1387C>T p.(Arg463Trp) - - - -
+?/+? - 2/5 c.1387C>T p.(Arg463Trp) possibly_damaging(0.846) missense_variant - deleterious(0.02)
./. - - c.1391T>C p.(Leu464Pro) - - - -
+/+ - 2/5 c.1422G>A p.(Trp474*) - stop_gained - -
./. - - c.1422G>A p.(Trp474*) - - - -
./. - 2/5 c.1422G>T p.(Trp474Cys) probably_damaging(0.98) missense_variant - deleterious(0)
./. - - c.1423G>C p.(Ala475Pro) - - - -
+/+ - 2/5 c.1423G>C p.(Ala475Pro) probably_damaging(0.972) missense_variant - deleterious(0.01)
./. - - c.1488T>C p.(=) - - - -
./. - - c.1523A>G p.(Tyr508Cys) - - - -
+/+ - 3/5 c.1523A>G p.(Tyr508Cys) probably_damaging(0.986) missense_variant - deleterious(0.01)
./. - - c.1527C>T p.(=) - - - -
./. - - c.1593-5C>T p.? - - - -
./. - - c.1593-3T>C p.? - - - -
./. - - c.1697A>G p.(Lys566Arg) - - - -
./. - - c.*30-14C>A p.(=) - - - -
./. - - c.*148C>T p.(=) - - - -
./. - - c.*270G>A p.(=) - - - -
./. - - c.*340G>A p.(=) - - - -
./. - - c.*345A>C p.(=) - - - -
./. - - c.*554G>A p.(=) - - - -
./. - - c.*584T>G p.(=) - - - -
./. - - c.*651C>T p.(=) - - - -
./. - - c.*717A>G p.(=) - - - -
./. - - c.*769A>T p.(=) - - - -
./. - - c.*788G>C p.(=) - - - -
./. - - c.*805C>T p.(=) - - - -
./. - - c.*821_*822del p.(=) - - - -
./. - - c.*871C>G p.(=) - - - -
./. - - c.*905G>A p.(=) - - - -
./. - - c.*924C>T p.(=) - - - -
./. - - c.*969G>A p.(=) - - - -
./. - - c.*1059C>G p.(=) - - - -
./. - - c.*1097C>G p.(=) - - - -
./. - - c.*1113T>C p.(=) - - - -
./. - - c.*1116A>T p.(=) - - - -
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