Transcript #00000228

Transcript name transcript variant 2
Gene name NUBPL (nucleotide binding protein-like)
Chromosome 14
Transcript - NCBI ID NM_001201573.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001188502.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

65 entries on 1 page. Showing entries 1 - 65.
Legend  

Affects function     

Location     

Exon     

AscendingDNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
./. - - c.23T>C p.(Leu8Pro) - - - -
+/+ - 2/9 c.25G>T - probably_damaging(1) missense_variant - deleterious(0)
./. - - c.25G>T p.(Asp9Tyr) - - - -
./. - - c.61A>G p.(Met21Val) - - - -
./. - - c.81G>A p.(=) - - - -
./. - - c.95G>A p.(Ser32Asn) - - - -
./. - - c.96C>T p.(=) - - - -
./. - - c.200C>T p.(Ser67Leu) - - - -
./. - - c.226-14T>C - - - - -
./. - - c.257T>C p.(Val86Ala) - - - -
./. - - c.285G>A p.(=) - - - -
./. - - c.291A>C p.(Leu97Phe) - - - -
./. - - c.305A>C p.(Asn102Thr) - - - -
./. - - c.315A>C p.(=) - - - -
./. - - c.351C>T p.(=) - - - -
./. - - c.373_374insGTGCTGCCTT p.(Glu127Alafs*4) - - - -
./. - - c.389G>A p.(Arg130His) - - - -
./. - - c.397C>T p.(His133Tyr) - - - -
./. - - c.405+1G>A p.? - - - -
./. - - c.527-27T>C p.(=) - - - -
+/+ - - c.527-27T>C - - - - -
./. - - c.606T>A p.(Asp202Glu) - - - -
./. - - 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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