Transcript #00017083 (NM_003738.4, PTCH2 gene)

Transcript name transcript variant 1
Gene name PTCH2 (patched 2)
Chromosome 1
Transcript - NCBI ID NM_003738.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_003729.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

72 entries on 1 page. Showing entries 1 - 72.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.44C>T r.(?) p.(Thr15Ile)
-/. - c.90G>A r.(?) p.(Leu30=)
./. - c.163T>C r.(?) p.(Cys55Arg)
-/. - c.265+13C>T r.(=) p.(=)
-?/. - c.354C>A r.(?) p.(Thr118=)
?/. - c.455A>T r.(?) p.(Lys152Met)
-?/. - c.455+16C>A r.(=) p.(=)
-?/. - c.455+16C>A r.(=) p.(=)
?/. - c.527T>G r.(?) p.(Met176Arg)
+?/. - c.528del r.(?) p.(Met176Ilefs*9)
?/. - c.530T>C r.(?) p.(Ile177Thr)
?/. - c.689C>T r.(?) p.(Ser230Phe)
?/. - c.703C>T r.(?) p.(Arg235Trp)
?/. - c.764C>G r.(?) p.(Pro255Arg)
-?/. - c.826G>A r.(?) p.(Ala276Thr)
-/. - c.840T>C r.(?) p.(Ser280=)
-/. - c.840T>C r.(?) p.(Ser280=)
-?/. - c.840T>C r.(?) p.(Ser280=)
-?/. - c.840T>C r.(?) p.(Ser280=)
?/. - c.1039C>T r.(?) p.(Gln347*)
?/. - c.1039C>T r.(?) p.(Gln347*)
-/. - c.1073G>A r.(?) p.(Arg358His)
-/. - c.1073G>A r.(?) p.(Arg358His)
-/. - c.1073G>A r.(?) p.(Arg358His)
-?/. - c.1080G>T r.(?) p.(Val360=)
-?/. - c.1080G>T r.(?) p.(Val360=)
-/. - c.1080G>T r.(?) p.(Val360=)
?/. - c.1083+3C>T r.spl? p.?
?/. - c.1172_1173del r.(?) p.(Ser391Ter)
-?/. - c.1191T>A r.(?) p.(Arg397=)
?/. - c.1223A>G r.(?) p.(Tyr408Cys)
?/. - c.1247G>A r.(?) p.(Trp416*)
?/. - c.1273G>A r.(?) p.(Val425Met)
-?/. - c.1284C>T r.(?) p.(Ala428=)
-?/. - c.1371+5G>A r.spl? p.?
-?/. - c.1380C>T r.(?) p.(Pro460=)
-?/. - c.1425G>A r.(?) p.(Ala475=)
./. - c.1568C>T r.(?) p.(Ala523Val)
./. - c.1568C>T r.(?) p.(Ala523Val)
-?/. - c.1593G>A r.(?) p.(Ala531=)
-?/. - c.1593G>A r.(?) p.(Ala531=)
-?/. - c.1596C>T r.(?) p.(Ala532=)
-?/. - c.1596C>T r.(?) p.(Ala532=)
?/. - c.1666C>T r.(?) p.(Arg556Trp)
-?/. - c.1692G>A r.(?) p.(Val564=)
-?/. - c.1720G>T r.(?) p.(Ala574Ser)
-?/. - c.1864C>A r.(?) p.(His622Asn)
-/. - c.1864C>A r.(?) p.(His622Asn)
-?/. - c.1864C>A r.(?) p.(His622Asn)
-/. - c.1864C>T r.(?) p.(His622Tyr)
?/. 14 c.1864C>T r.(?) p.(His622Tyr)
-?/. - c.1864C>T r.(?) p.(His622Tyr)
-?/. - c.2013C>T r.(?) p.(Phe671=)
-/. - c.2055T>C r.(?) p.(Ala685=)
-/. - c.2127C>T r.(?) p.(Asp709=)
-/. - c.2127C>T r.(?) p.(Asp709=)
-?/. - c.2184C>T r.(?) p.(Ser728=)
-/. - c.2355C>T r.(?) p.(Tyr785=)
?/. - c.2356C>T r.(?) p.(Arg786Cys)
?/. - c.2357G>C r.(?) p.(Arg786Pro)
?/. - c.2389G>A r.(?) p.(Asp797Asn)
-/. - c.2427G>C r.(?) p.(Ser809=)
-/. - c.2427G>C r.(?) p.(Ser809=)
-/. - c.2487C>T r.(?) p.(Asp829=)
-?/. - c.2679G>A r.(?) p.(Thr893=)
-/. - c.2963C>T r.(?) p.(Thr988Met)
?/. - c.3055G>A r.(?) p.(Val1019Met)
?/. - c.3055G>A r.(?) p.(Val1019Met)
-?/. - c.3189C>T r.(?) p.(Thr1063=)
?/. - c.3210G>C r.(?) p.(Leu1070Phe)
?/. - c.3289C>T r.(?) p.(Leu1097Phe)
-?/. - c.3545C>T r.(?) p.(Pro1182Leu)
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