Transcript #00006306 (NM_001083602.1, PTCH1 gene)

Transcript name transcript variant 1a
Gene name PTCH1 (patched 1)
Chromosome 9
Transcript - NCBI ID NM_001083602.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001077071.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-30 11:20:09 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-206_-205insGAA -206 r.(=) p.(=) - utr-5 -
./. - c.-206_-205insGAA -206 r.(=) p.(=) - utr-5 -
./. - c.-187G>C -187 r.(=) p.(=) - utr-5 -
./. - c.1306-8T>C 1306 r.(=) p.(=) - splice 8
./. - c.1306-8T>C 1306 r.(=) p.(=) - splice 8
./. - c.1467T>C 1467 r.(?) p.(=) - coding-synonymous -
./. - c.1467T>C 1467 r.(?) p.(=) - coding-synonymous -
./. - c.1467T>C 1467 r.(?) p.(=) - coding-synonymous -
./. - c.1467T>C 1467 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1488C>T 1488 r.(?) p.(=) - coding-synonymous -
./. - c.1611C>T 1611 r.(?) p.(=) - coding-synonymous -
./. - c.1611C>T 1611 r.(?) p.(=) - coding-synonymous -
./. - c.1611C>T 1611 r.(?) p.(=) - coding-synonymous -
./. - c.1649+14C>T 1649 r.(=) p.(=) - intron 14
./. - c.1656C>T 1656 r.(?) p.(=) - coding-synonymous -
./. - c.1656C>T 1656 r.(?) p.(=) - coding-synonymous -
./. - c.1656C>T 1656 r.(?) p.(=) - coding-synonymous -
./. - c.1985C>T 1985 r.(?) p.(Thr662Met) - missense -
./. - c.1985C>T 1985 r.(?) p.(Thr662Met) - missense -
./. - c.2052+25T>C 2052 r.(=) p.(=) - intron 25
./. - c.2052+25T>C 2052 r.(=) p.(=) - intron 25
./. - c.2052+25T>C 2052 r.(=) p.(=) - intron 25
./. - c.2052+25T>C 2052 r.(=) p.(=) - intron 25
./. - c.2052+25T>C 2052 r.(=) p.(=) - intron 25
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+9G>C 2362 r.(=) p.(=) - intron 9
./. - c.2362+45T>C 2362 r.(=) p.(=) - intron 45
./. - c.2363-36G>A 2363 r.(=) p.(=) - intron 36
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2689+21A>G 2689 r.(=) p.(=) - intron 21
./. - c.2943T>G 2943 r.(?) p.(=) - coding-synonymous -
./. - c.2943T>G 2943 r.(?) p.(=) - coding-synonymous -
./. - c.2943T>G 2943 r.(?) p.(=) - coding-synonymous -
./. - c.2943T>G 2943 r.(?) p.(=) - coding-synonymous -
./. - c.2952C>T 2952 r.(?) p.(=) - coding-synonymous -
./. - c.3385A>T 3385 r.(?) p.(Thr1129Ser) - missense -
./. - c.3385A>T 3385 r.(?) p.(Thr1129Ser) - missense -
./. - c.3385A>T 3385 r.(?) p.(Thr1129Ser) - missense -
./. - c.3385A>T 3385 r.(?) p.(Thr1129Ser) - missense -
./. - c.3385A>T 3385 r.(?) p.(Thr1129Ser) - missense -
./. - c.3385A>T 3385 r.(?) p.(Thr1129Ser) - missense -
./. - c.3607-9C>T 3607 r.(=) p.(=) - intron 9
./. - c.3607-9C>T 3607 r.(=) p.(=) - intron 9
./. - c.3607-9C>T 3607 r.(=) p.(=) - intron 9
./. - c.3709C>T 3709 r.(?) p.(Arg1237Cys) - missense -
./. - c.3746C>T 3746 r.(?) p.(Pro1249Leu) - missense -
./. - c.3746C>T 3746 r.(?) p.(Pro1249Leu) - missense -
./. - c.3746C>T 3746 r.(?) p.(Pro1249Leu) - missense -
./. - c.3746C>T 3746 r.(?) p.(Pro1249Leu) - missense -
./. - c.3746C>T 3746 r.(?) p.(Pro1249Leu) - missense -
./. - c.3746C>T 3746 r.(?) p.(Pro1249Leu) - missense -
./. - c.3746C>T 3746 r.(?) p.(Pro1249Leu) - missense -
./. - c.3746C>T 3746 r.(?) p.(Pro1249Leu) - missense -
./. - c.3746C>T 3746 r.(?) p.(Pro1249Leu) - missense -
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