Transcript #00014659 (NM_201631.3, TGM5 gene)

Transcript name transcript variant 1
Gene name TGM5 (transglutaminase 5)
Chromosome 15
Transcript - NCBI ID NM_201631.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_963925.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

50 entries on 1 page. Showing entries 1 - 50.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.10+11C>T 10 r.(=) p.(=) - intron 11
./. - c.10+11C>T 10 r.(=) p.(=) - intron 11
./. - c.44C>G 44 r.(?) p.(Ser15Cys) - missense -
./. - c.44C>G 44 r.(?) p.(Ser15Cys) - missense -
./. - c.314G>A 314 r.(?) p.(Cys105Tyr) - missense -
./. - c.654C>T 654 r.(?) p.(=) - coding-synonymous -
./. - c.654C>T 654 r.(?) p.(=) - coding-synonymous -
./. - c.654C>T 654 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.660C>T 660 r.(?) p.(=) - coding-synonymous -
./. - c.862+24A>G 862 r.(=) p.(=) - intron 24
./. - c.863-50G>C 863 r.(=) p.(=) - intron 50
./. - c.1055C>G 1055 r.(?) p.(Ala352Gly) - missense -
./. - c.1055C>G 1055 r.(?) p.(Ala352Gly) - missense -
./. - c.1055C>G 1055 r.(?) p.(Ala352Gly) - missense -
./. - c.1055C>G 1055 r.(?) p.(Ala352Gly) - missense -
./. - c.1055C>G 1055 r.(?) p.(Ala352Gly) - missense -
./. - c.1055C>G 1055 r.(?) p.(Ala352Gly) - missense -
./. - c.1055C>G 1055 r.(?) p.(Ala352Gly) - missense -
./. - c.1055C>G 1055 r.(?) p.(Ala352Gly) - missense -
./. - c.1055C>G 1055 r.(?) p.(Ala352Gly) - missense -
./. - c.1106-7C>T 1106 r.(=) p.(=) - splice 7
./. - c.1510G>A 1510 r.(?) p.(Val504Met) - missense -
./. - c.1510G>A 1510 r.(?) p.(Val504Met) - missense -
./. - c.1510G>A 1510 r.(?) p.(Val504Met) - missense -
./. - c.1513G>A 1513 r.(?) p.(Val505Met) - missense -
./. - c.1632T>G 1632 r.(?) p.(Ser544Arg) - missense -
./. - c.1822A>G 1822 r.(?) p.(Lys608Glu) - missense -
./. - c.1822A>G 1822 r.(?) p.(Lys608Glu) - missense -
./. - c.*23G>A 2186 r.(=) p.(=) - utr-3 -
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