Transcript #00000227

Transcript name transcript variant 1
Gene name NUBPL (nucleotide binding protein-like)
Chromosome 14
Transcript - NCBI ID NM_025152.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_079428.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

80 entries on 1 page. Showing entries 1 - 80.
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Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.-39G>A p.(=) - - - -
./. - - c.-25A>G p.(=) - - - -
./. - - c.-13A>G p.(=) - - - -
./. - - c.-7C>T p.(=) - - - -
./. - - c.-1C>T p.(=) - - - -
./. - - c.2T>C p.? - - - -
./. - - c.46C>T p.(Arg16Trp) - - - -
./. - - c.77G>T p.(Gly26Val) - - - -
./. - - c.109-11A>T p.(=) - - - -
./. - - c.162C>T p.(=) - - - -
./. - - c.166G>A p.(Gly56Arg) - - - -
+/+ - 2/6 c.166G>A p.(Gly56Arg) unknown(0) missense_variant - deleterious(0)
./. - - c.199A>G p.(Lys67Glu) - - - -
./. - - c.285C>T p.(=) - - - -
./. - - c.286G>A p.(Asp96Asn) - - - -
./. - - c.311T>C p.(Leu104Pro) - - - -
./. - - c.313G>T p.(Asp105Tyr) - - - -
+/+ - 4/10 c.313G>T p.(Asp105Tyr) probably_damaging(1) missense_variant,NMD_transcript_variant - deleterious(0)
./. - - c.349A>G p.(Met117Val) - - - -
./. - - c.369G>A p.(=) - - - -
./. - - c.383G>A p.(Ser128Asn) - - - -
./. - - c.384C>T p.(=) - - - -
./. - - c.488C>T p.(Ser163Leu) - - - -
./. - - c.514-14T>C p.(=) - - - -
./. - - c.545T>C p.(Val182Ala) - - - -
./. - - c.573G>A p.(=) - - - -
./. - - c.579A>C p.(Leu193Phe) - - - -
./. - - c.593A>C p.(Asn198Thr) - - - -
./. - - c.603A>C p.(=) - - - -
./. - - c.639C>T p.(=) - - - -
./. - - c.661_662insGTGCTGCCTT p.(Glu223Alafs*4) - - - -
./. - - c.677G>A p.(Arg226His) - - - -
./. - - c.685C>T p.(His229Tyr) - - - -
./. - - c.693+1G>A p.? - - - -
./. - - c.815-27T>C p.(=) - - - -
+/+ - - c.815-27T>C p.(=) - - - -
./. - - c.894T>A p.(Asp298Glu) - - - -
./. - - c.*122G>C p.(=) - - - -
./. - - c.*135T>G p.(=) - - - -
./. - - c.*188T>C p.(=) - - - -
./. - - c.*273C>T p.(=) - - - -
./. - - c.*312G>A p.(=) - - - -
./. - - c.*355T>C p.(=) - - - -
./. - - c.*357C>G p.(=) - - - -
./. - - c.*444C>T p.(=) - - - -
./. - - c.*527G>A p.(=) - - - -
./. - - c.*536_*537insA p.(=) - - - -
./. - - c.*561G>A p.(=) - - - -
./. - - c.*638C>G p.(=) - - - -
./. - - c.*836C>G p.(=) - - - -
./. - - c.*905A>C p.(=) - - - -
./. - - c.*995T>C p.(=) - - - -
./. - - c.*1015C>A p.(=) - - - -
./. - - c.*1048G>A p.(=) - - - -
./. - - c.*1053G>A p.(=) - - - -
./. - - c.*1119_*1120insA p.(=) - - - -
./. - - c.*1120_*1121insT p.(=) - - - -
./. - - c.*1121_*1122insC p.(=) - - - -
./. - - c.*1121_*1123del p.(=) - - - -
./. - - c.*1122_*1123insA p.(=) - - - -
./. - - c.*1122_*1124del p.(=) - - - -
./. - - c.*1123_*1126del p.(=) - - - -
./. - - c.*1145_*1148del p.(=) - - - -
./. - - c.*1146_*1148del p.(=) - - - -
./. - - c.*1148del p.(=) - - - -
./. - - c.*1149_*1150insA p.(=) - - - -
./. - - c.*1150_*1151insG p.(=) - - - -
./. - - c.*1151G>A p.(=) - - - -
./. - - c.*1260T>C p.(=) - - - -
./. - - c.*1451C>T p.(=) - - - -
./. - - c.*1609G>A p.(=) - - - -
./. - - c.*1619C>T p.(=) - - - -
./. - - c.*1685A>G p.(=) - - - -
./. - - c.*1694G>A p.(=) - - - -
./. - - c.*1773A>G p.(=) - - - -
./. - - c.*1776G>A p.(=) - - - -
./. - - c.*1840A>G p.(=) - - - -
./. - - c.*1874A>G p.(=) - - - -
./. - - c.*1888G>A p.(=) - - - -
./. - - c.*2036A>C p.(=) - - - -
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