Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TNN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175079569:175079569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646G>A
AA Mutation	p.Val216Met(p.V216M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175080373:175080373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780402309
CDS Mutation	c.995G>A
AA Mutation	p.Arg332His(p.R332H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175093999:175093999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1334G>T
AA Mutation	p.Ser445Ile(p.S445I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000239462
Start	175144548:175144548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3757G>A
AA Mutation	p.Glu1253Lys(p.E1253K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175116968:175116968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772006145
CDS Mutation	c.2149G>A
AA Mutation	p.Asp717Asn(p.D717N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175128037:175128037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3051G>A
AA Mutation	p.Met1017Ile(p.M1017I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175097635:175097635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1807C>A
AA Mutation	p.Gln603Lys(p.Q603K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175094233:175094233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1568C>T
AA Mutation	p.Ala523Val(p.A523V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175098399:175098399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1923C>A
AA Mutation	p.Asp641Glu(p.D641E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175077423:175077423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5G>A
AA Mutation	p.Ser2Asn(p.S2N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175126978:175126978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767983713
CDS Mutation	c.2938C>T
AA Mutation	p.Arg980Cys(p.R980C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175080415:175080415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037T>C
AA Mutation	p.Leu346Pro(p.L346P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175094041:175094041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376C>A
AA Mutation	p.Ala459Glu(p.A459E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175123501:175123501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116607864
CDS Mutation	c.2752C>T
AA Mutation	p.Arg918Cys(p.R918C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175098585:175098585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109G>T
AA Mutation	p.Lys703Asn(p.K703N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175118717:175118717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2543G>A
AA Mutation	p.Ser848Asn(p.S848N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000239462
Start	175097417:175097417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589A>G
AA Mutation	p.Glu530Gly(p.E530G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175094013:175094013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1348G>C
AA Mutation	p.Val450Leu(p.V450L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175097674:175097674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1846G>A
AA Mutation	p.Ala616Thr(p.A616T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175123447:175123447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750616827
CDS Mutation	c.2698A>G
AA Mutation	p.Met900Val(p.M900V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175097465:175097465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1637C>G
AA Mutation	p.Thr546Ser(p.T546S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175117040:175117040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371486038
CDS Mutation	c.2221C>T
AA Mutation	p.Arg741Cys(p.R741C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175083860:175083860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1159C>G
AA Mutation	p.Pro387Ala(p.P387A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175118732:175118732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761263903
CDS Mutation	c.2558C>T
AA Mutation	p.Thr853Met(p.T853M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175135857:175135857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546877646
CDS Mutation	c.3343C>T
AA Mutation	p.Arg1115Trp(p.R1115W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175079522:175079522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775730066
CDS Mutation	c.599C>T
AA Mutation	p.Pro200Leu(p.P200L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175098426:175098426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759866598
CDS Mutation	c.1950C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175123605:175123605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138474300
CDS Mutation	c.2856C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175098387:175098387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780062151
CDS Mutation	c.1911G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175079628:175079628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175128067:175128067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368089539
CDS Mutation	c.3081G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175077715:175077715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747692641
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175097664:175097664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1836T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175098435:175098435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1959C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175077547:175077547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201267863
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000239462
Start	175144385:175144386(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3596-2_3596-1insT
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000239462
Start	175097416:175097416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1589-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TNN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175083852:175083852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1151G>A
AA Mutation	p.Arg384Gln(p.R384Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175098338:175098338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771337724
CDS Mutation	c.1862A>G
AA Mutation	p.Asp621Gly(p.D621G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175077664:175077664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.246G>T
AA Mutation	p.Gln82His(p.Q82H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175118633:175118633(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2459T>C
AA Mutation	p.Val820Ala(p.V820A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175080333:175080333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955C>A
AA Mutation	p.Leu319Ile(p.L319I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175083793:175083793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1092G>T
AA Mutation	p.Glu364Asp(p.E364D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000239462
Start	175123417:175123417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2668A>C
AA Mutation	p.Asn890His(p.N890H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175098432:175098432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1956G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000239462
Start	175077715:175077715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747692641
CDS Mutation	c.297C>T
Mutation Classification	Silent
Feature Type	Transcript