Transcript #00000007 (NM_004415.2, DSP gene)

Transcript name transcript variant 1
Gene name DSP (desmoplakin)
Chromosome 6
Transcript - NCBI ID NM_004415.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_004406.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 24 c.? - p.Phe2885Phe
./. 01 c.1delA - p.Met1fsX
./. 01 c.1dup - p.Met1extMet-Asnfs
./. 01 c.88G>A - p.Val30Met
./. 01 c.137G>A - p.Gly46Asp
./. 01 c.145A>G - p.Thr49Ala
./. 01 c.146C>T - p.Thr49Ile
./. 02 c.242G>A - p.Cys81Tyr
./. 02 c.269A>G - p.Gln90Arg
./. 03 c.344A>G - p.Asn115Ser
./. 04 c.423-1G>A - -
./. 04 c.596G>A - p.Arg199Lys
./. 05 c.643G>A - p.Glu215Lys
./. 05 c.688G>A - p.Asp230Asn
./. 05 c.699G>A - p.Trp233X
./. 07 c.782C>T - p.Ala261Val
./. 07 c.853T>G - p.Trp285Gly
./. 07 c.860A>G - p.Asn287Ser
./. 07 c.861T>G - p.Asn287Lys
./. 07 c.861T>G - p.Asn287Lys
./. 07 c.861T>G - p.Asn287Lys
./. 07 c.895A>C - p.Ser299Arg
./. 07 c.895A>C - p.Ser299Arg
./. 07 c.897C>G - p.Ser299Arg
./. 07 c.913A>T - p.Ile305Phe
./. 07 c.939+1G>A - -
./. 07 c.939+1G>A - -
./. 08 c.961G>C - p.Val321Leu
./. 08 c.971A>G - p.Lys324Arg
./. 08 c.976C>T - p.Leu326Phe
./. 08 c.991C>T - p.Gln331X
./. 08 c.991C>T - p.Gln331X
./. 09 c.1103T>C - p.Ile368Thr
./. 09 c.1136T>C - p.Phe379Ser
./. 10 c.1154C>T - p.Ala385Val
./. 10 c.1222A>C - p.Asn408His
./. 11 c.1333A>G - p.Ile445Val
./. 12 c.1423del - p.Ile475SerfsX10
./. 12 c.1481A>T - p.Tyr494Phe
./. 12 c.1563C>A - p.Asp521Glu
./. 13 c.1696G>A - p.Ala566Thr
./. 14 c.1730T>C - p.Met577Thr
./. 14 c.1778A>G - p.Asn593Ser
./. 14 c.1790C>T - p.Ser597Leu
./. 14 c.1817_1846dup - P.Arg606_Ala615dup
./. 14 c.1901C>G - p.Thr634Arg
./. 15 c.1949A>G - p.Asn650Ser
./. 15 c.1963A>T - p.Ile655Phe
./. 15 c.1990C>T - p.Gln664X
./. 15 c.1990C>T - p.Gln664X
./. 15 c.1990C>T - p.Gln664X
./. 15 c.2023A>G - p.Ile675Val
./. 15 c.2033A>G - p.Gln678Arg
./. 15 c.2037A>G - p.Ile679Met
./. 16 c.2288A>G - p.Tyr763Cys
./. 17 c.2422C>T - p.Arg808Cys
./. 17 c.2427T>A - p.Cys809X
./. 17 c.2427T>A - p.Cys809X
./. 17 c.2427T>A - p.Cys809X
./. 18 c.2468C>T - p.Ser823Leu
./. 18 c.2516_2519del - p.His839LeufsX24
./. 18 c.2525C>T - p.Thr842Ile
./. 18 c.2552T>A - p.Leu851Gln
./. 18 c.2596C>T - p.Arg866Cys
./. 19 c.2631G>A - p.Arg877Arg
./. 19 c.2631G>A - p.Arg877=
./. 19 c.2723G>A - p.Arg908His
./. 19 c.2773C>T - p.Arg925Trp
./. 19 c.2774G>A - p.Arg925Gln
./. 20 c.2815G>A - p.Gly939Ser
./. 20 c.2815G>A - p.Gly939Ser
./. 20 c.2862C>T - p.Cys954Cys
./. 20 c.2875_2877+2delAAGGT - -
./. 22 c.3053G>C - p.Ser1018Thr
./. 23 c.3282G>C - p.Lys1094Asn
./. 23 c.3304G>A - p.Gly1102Arg
./. 23 c.3551G>A - p.Arg1184Gln
./. 23 c.3562T>C - p.Tyr1188His
./. 23 c.3616T>A - p.Leu1206Ile
./. 23 c.3764G>A - p.Arg1255Lys
./. 23 c.3799C>T - p.Arg1267X
./. 23 c.3862A>C - p.Lys1288Gln
./. 23 c.3887A>G - p.Lys1296Arg
./. 23 c.3901C>T - p.Gln1301X
./. 23 c.3904C>T - p.Arg1302Cys
./. 23 c.3922C>T - p.Arg1308Trp
./. 23 c.3923G>A - p.Arg1308Gln
./. 23 c.3956C>T - p.Thr1319Ile
./. 23 c.3963G>A - p.Gln1321=
./. 23 c.3971_3974del - p.Asn1324ArgfsX24
./. 23 c.3973A>C - p.Lys1325Gln
./. 23 c.3995_3996delinsAATCGA - p.Ala1332GlufsX15
./. 23 c.4022G>A - p.Arg1341His
./. 23 c.4046G>A - p.Ser1349Asn
./. 23 c.4105G>A - p.Glu1369Lys
./. 23 c.4141A>T - p.Thr1381Ser
./. 23 c.4173C>A - p.Tyr1391Ter
./. 23 c.4180C>T - p.Gln1394Ter
./. 23 c.4372C>G - p.Arg1458Gly
./. 23 c.4455G>T - p.Arg1485Ser
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