Transcript #00000102 (NM_001012331.1, NTRK1 gene)

Transcript name neurotrophic tyrosine kinase, receptor, type 1
Gene name NTRK1 (neurotrophic tyrosine kinase, receptor, type 1)
Chromosome 1
Transcript - NCBI ID NM_001012331.1
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 13 c.1615 - -
./. 01 c.25C>T - p.Gln9X
./. 01 c.53G>A - p.Gly18Glu
./. 01 c.55_56insG - p.Pro19ArgfsX40
./. 01 c.202delC - p.Asn67fsX1
./. 02 c.236T>A - p.Leu79Gln
./. 02 c.239A>G - p.Gln80Arg
./. 02 c.253C>A - p.Arg85Ser
./. 02 c.254G>A - p.Arg85His
./. 02 c.265G>A - p.Gly89Ser
./. 02 c.271G>C - p.Gly91Arg
./. 02 c.287+2dupT - p.?
./. 03 c.326A>G - p.Asp109Gly
./. 03 c.353_359+2delGTCGCCTGT - -
./. 03 c.359+5G>T - -
./. 04 c.391_392del - p.Ser131LeufsX41
./. 04 c.391_392delTC - p.Ser131LeufsX41
./. 05 c.437C>T - p.Ser146Leu
./. 05 c.446C>A - p.Pro149His
./. 05 c.469C>T - p.Arg157Cys
./. 05 c.470G>A - p.Arg157His
./. 05 c.482G>A - p.Arg161His
./. 05 c.482G>A - p.Arg161His
./. 05 c.496G>T - p.Gly166X
./. 05 c.505G>A - p.Gly169Arg
./. 05 c.526C>T - p.Gln176X
./. 05 c.543del - p.Leu183TrpfsX14
./. 05 c.550G>T - p.Ala184Ser
./. 05 c.570C>G - p.Ser190Arg
./. 06 c.611C>T - p.Ser204Leu
./. 06 c.638T>C - p.Leu213Pro
./. 06 c.638T>C - p.Leu213Pro
./. 06 c.638T>C - p.Leu213Pro
./. 06 c.657dup - p.Arg220AlafsX38
./. 06 c.710C>T - p.Thr237Met
./. 06 c.713T>G - p.Val238Gly
./. 06 c.717+1G>C - -
./. 07 c.722_723insC - p.Gly242TrpfsX16
./. 07 c.778A>G - p.Arg260Gly
./. 07 c.808G>A - p.Asp270Asn
./. 07 c.817C>T - p.Arg273Trp
./. 07 c.824A>C - p.Glu275Ala
./. 08 c.851-33T>A - p.?
./. 08 c.854C>T - p.Pro285Leu
./. 08 c.865C>A - p.Gln289Lys
./. 08 c.924_930delGCCGGCA - p.Gln308HisfsX154
./. 08 c.940C>T - p.Arg314Cys
./. 08 c.1021G>A - p.Val341Met
./. 08 c.1037T>C - p.Leu346Pro
./. 08 c.1076A>G - p.Tyr359Cys
./. 08 c.1139A>G - p.Asp380Gly
./. 08 c.1166del - p.Asp389AlafsX75
./. 09 c.1202delC - p.Pro407ArgfsX63
./. 10 c.1234-1G>A - -
./. 10 c.1264G>T - p.Ala422Ser
./. 10 c.1291C>T - p.Leu431Phe
./. 10 c.1302C>G - p.Asn434Lys
./. 10 c.1313G>A - p.Arg438Gln
./. 10 c.1324T>C - p.Phe442Leu
./. 10 c.1336C>T - p.Arg446Cys
./. 11 c.1420G>A - p.Glu474Lys
./. 11 c.1447C>T - p.His483Tyr
./. 11 c.1456G>A - p.Glu486Lys
./. 12 c.1504_1505delCG - p.Ile504MetfsX40
./. 12 c.1506_1513dup - p.Val505GlyfsX39
./. 12 c.1534dup - p.Glu512GlyfsX11
./. 13 c.1642delC - p.Arg548GlyfsX104
./. 13 c.1645_1646insG - p.Gln549ArgfsX6
./. 13 c.1660G>A - p.Glu554Lys
./. 13 c.1679T>C - p.Met560Thr
./. 13 c.1711G>C - p.Gly571Arg
./. 13 c.1711G>C - p.Gly571Arg
./. 13 c.1723G>A - p.Glu575Lys
./. 13 c.1725G>A - p.Glu575Glu
./. 13 c.1736delT - p.Leu579ArgfsX73
./. 14 c.1792C>T - p.His598Tyr
./. 14 c.1796G>C - p.Gly599Ala
./. 14 c.1820G>T - p.Gly607Val
./. 14 c.1820G>T - p.Gly607Val
./. 14 c.1820G>T - p.Gly607Val
./. 14 c.1823G>T - p.Gly608Val
./. 14 c.1825G>C - p.Glu609Gln
./. 14 c.1831G>T - p.Val611Leu
./. 14 c.1841_1842insT - p.Gly614GlyfsX11
./. 14 c.1852C>T - -
./. 14 c.1858_1859insG - p.Gln620ArgfsX7
./. 14 c.1869C>T - -
./. 14 c.1873G>C - p.Ala625Pro
./. 14 c.1877_1878insA - p.Ser626ArgfsX37
./. 14 c.1903delC - p.Leu635TrpfsX17
./. 14 c.1921G>T - p.Val641Leu
./. 14 c.1927C>T - p.Arg643Trp
./. 14 c.1927C>T - p.Arg643Trp
./. 14 c.2002G>T - p.Asp668Tyr
./. 15 c.2031G>C - -
./. 15 c.2034A>G - -
./. 15 c.2038C>A - p.Arg680Gly
./. 15 c.2066C>T - Pro689Leu
./. 15 c.2066C>T - p.Pro689Leu
./. 15 c.2086_2087 ins C - p.Arg696ProfsX2
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