Colon Cancer: Gene >> MCC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113082890:113082890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184A>T
AA Mutation	p.Glu395Val(p.E395V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113151367:113151367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757596340
CDS Mutation	c.113G>A
AA Mutation	p.Arg38His(p.R38H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113068103:113068103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769744769
CDS Mutation	c.1436C>T
AA Mutation	p.Ala479Val(p.A479V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113104233:113104233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580C>A
AA Mutation	p.Gln194Lys(p.Q194K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113064125:113064125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149204864
CDS Mutation	c.1502G>A
AA Mutation	p.Arg501Gln(p.R501Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113122755:113122755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.386G>A
AA Mutation	p.Arg129Gln(p.R129Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113071166:113071166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283C>T
AA Mutation	p.Ala428Val(p.A428V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113049223:113049223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751790153
CDS Mutation	c.1955C>T
AA Mutation	p.Thr652Met(p.T652M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113043575:113043575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2141G>T
AA Mutation	p.Cys714Phe(p.C714F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113101752:113101752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815G>A
AA Mutation	p.Arg272Gln(p.R272Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000408903
Start	113385075:113385075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308A>G
AA Mutation	p.Glu103Gly(p.E103G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113085228:113085228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369421434
CDS Mutation	c.911C>T
AA Mutation	p.Pro304Leu(p.P304L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113027309:113027309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367917509
CDS Mutation	c.2483C>T
AA Mutation	p.Ser828Leu(p.S828L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113101921:113101921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.646C>T
AA Mutation	p.Leu216Phe(p.L216F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000408903
Start	113340691:113340691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455C>A
AA Mutation	p.Ser152Tyr(p.S152Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000408903
Start	113385020:113385020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363G>T
AA Mutation	p.Lys121Asn(p.K121N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000408903
Start	113488290:113488290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370355557
CDS Mutation	c.125G>A
AA Mutation	p.Arg42His(p.R42H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113143303:113143303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563599843
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Cys(p.R77C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000408903
Start	113385004:113385004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.379A>G
AA Mutation	p.Ile127Val(p.I127V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113143239:113143239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199564726
CDS Mutation	c.293G>A
AA Mutation	p.Arg98His(p.R98H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113053908:113053908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368313454
CDS Mutation	c.1695C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113085281:113085281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369354056
CDS Mutation	c.858C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113085170:113085170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763704088
CDS Mutation	c.969C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113068147:113068147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144615351
CDS Mutation	c.1392G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000408903
Start	113340567:113340567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113104279:113104279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.534G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000302475
Start	113101817:113101817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.750C>A
AA Mutation	p.Cys250Ter(p.C250*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MCC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113071164:113071164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs578122540
CDS Mutation	c.1285G>A
AA Mutation	p.Glu429Lys(p.E429K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000302475
Start	113068182:113068182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773355443
CDS Mutation	c.1357G>A
AA Mutation	p.Glu453Lys(p.E453K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113068101:113068101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1438G>T
AA Mutation	p.Ala480Ser(p.A480S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000302475
Start	113151320:113151320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160G>T
AA Mutation	p.Ala54Ser(p.A54S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000302475
Start	113028960:113028960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2283C>T
Mutation Classification	Silent
Feature Type	Transcript