Colon Cancer: Gene >> TCHH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110759:152110759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146186285
CDS Mutation	c.2458C>T
AA Mutation	p.Arg820Trp(p.R820W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111854:152111854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1363C>T
AA Mutation	p.Arg455Cys(p.R455C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112711:152112711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506G>A
AA Mutation	p.Arg169His(p.R169H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107852:152107852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750681612
CDS Mutation	c.5365C>T
AA Mutation	p.Arg1789Cys(p.R1789C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109886:152109886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3331C>T
AA Mutation	p.Arg1111Trp(p.R1111W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111542:152111542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1675G>A
AA Mutation	p.Glu559Lys(p.E559K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108472:152108472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4745G>A
AA Mutation	p.Arg1582His(p.R1582H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108035:152108035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5182G>A
AA Mutation	p.Glu1728Lys(p.E1728K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108488:152108488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4729C>T
AA Mutation	p.Arg1577Cys(p.R1577C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108354:152108354(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4863C>A
AA Mutation	p.Phe1621Leu(p.F1621L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108725:152108725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4492G>C
AA Mutation	p.Glu1498Gln(p.E1498Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111557:152111557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543956977
CDS Mutation	c.1660G>A
AA Mutation	p.Glu554Lys(p.E554K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111655:152111655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772615095
CDS Mutation	c.1562G>A
AA Mutation	p.Arg521His(p.R521H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111929:152111929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288G>A
AA Mutation	p.Glu430Lys(p.E430K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112418:152112418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.799C>T
AA Mutation	p.Arg267Trp(p.R267W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112837:152112837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.380G>A
AA Mutation	p.Arg127Lys(p.R127K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109730:152109730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3487C>T
AA Mutation	p.Arg1163Cys(p.R1163C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107440:152107440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201507732
CDS Mutation	c.5777G>A
AA Mutation	p.Arg1926His(p.R1926H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108352:152108352(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4865G>A
AA Mutation	p.Arg1622His(p.R1622H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111368:152111368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1849G>A
AA Mutation	p.Glu617Lys(p.E617K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152113014:152113014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.203G>A
AA Mutation	p.Arg68His(p.R68H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107677:152107677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763314606
CDS Mutation	c.5540C>T
AA Mutation	p.Ala1847Val(p.A1847V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112313:152112313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Cys(p.R302C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111194:152111194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2023G>A
AA Mutation	p.Glu675Lys(p.E675K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109359:152109359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3858G>T
AA Mutation	p.Trp1286Cys(p.W1286C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112819:152112819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398C>T
AA Mutation	p.Pro133Leu(p.P133L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152109705:152109705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3512G>A
AA Mutation	p.Arg1171His(p.R1171H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110564:152110564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2653C>T
AA Mutation	p.Arg885Cys(p.R885C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108367:152108367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370364413
CDS Mutation	c.4850G>A
AA Mutation	p.Arg1617His(p.R1617H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111217:152111217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2000G>T
AA Mutation	p.Arg667Met(p.R667M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107627:152107627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5590C>A
AA Mutation	p.Leu1864Ile(p.L1864I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107971:152107971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5246T>C
AA Mutation	p.Ile1749Thr(p.I1749T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108475:152108475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4742T>C
AA Mutation	p.Phe1581Ser(p.F1581S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107849:152107849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5368A>G
AA Mutation	p.Ser1790Gly(p.S1790G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112819:152112819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398C>G
AA Mutation	p.Pro133Arg(p.P133R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110310:152110310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2907G>T
AA Mutation	p.Lys969Asn(p.K969N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110243:152110243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2974G>A
AA Mutation	p.Glu992Lys(p.E992K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112433:152112433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.784G>A
AA Mutation	p.Glu262Lys(p.E262K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152111163:152111163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2054T>A
AA Mutation	p.Leu685Gln(p.L685Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108770:152108770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765371735
CDS Mutation	c.4447C>T
AA Mutation	p.Arg1483Cys(p.R1483C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152107947:152107947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5270C>T
AA Mutation	p.Pro1757Leu(p.P1757L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110168:152110168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3049G>A
AA Mutation	p.Glu1017Lys(p.E1017K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152109212:152109212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4005C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152107403:152107403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5814A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152111672:152111672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1545C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152113010:152113010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.207C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152108222:152108222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4995C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152109937:152109937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3280C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	49
Mutation Consequence	stop_gained
Transcription ID	ENST00000368804
Start	152110974:152110974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2243G>A
AA Mutation	p.Trp748Ter(p.W748*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	50
Mutation Consequence	stop_gained
Transcription ID	ENST00000368804
Start	152110045:152110045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3172C>T
AA Mutation	p.Gln1058Ter(p.Q1058*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TCHH

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108761:152108761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4456A>G
AA Mutation	p.Lys1486Glu(p.K1486E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152110289:152110289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2928G>T
AA Mutation	p.Glu976Asp(p.E976D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152108923:152108923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4294T>A
AA Mutation	p.Phe1432Ile(p.F1432I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112635:152112635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582G>C
AA Mutation	p.Gln194His(p.Q194H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368804
Start	152112406:152112406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811C>T
AA Mutation	p.Leu271Phe(p.L271F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152112347:152112347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368804
Start	152109524:152109524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3693A>G
Mutation Classification	Silent
Feature Type	Transcript