Colon Cancer: Gene >> CORIN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47600243:47600243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2917T>C
AA Mutation	p.Tyr973His(p.Y973H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47763536:47763536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200249247
CDS Mutation	c.460G>A
AA Mutation	p.Ala154Thr(p.A154T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47665071:47665071(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550A>C
AA Mutation	p.Lys517Thr(p.K517T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47641968:47641968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748852470
CDS Mutation	c.2150G>A
AA Mutation	p.Gly717Asp(p.G717D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47603592:47603592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571162211
CDS Mutation	c.2617C>T
AA Mutation	p.Arg873Cys(p.R873C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47641974:47641974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2144C>T
AA Mutation	p.Ala715Val(p.A715V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47680212:47680212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147781342
CDS Mutation	c.1061G>A
AA Mutation	p.Arg354His(p.R354H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47603486:47603486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2723T>A
AA Mutation	p.Val908Asp(p.V908D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47661796:47661796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1650G>T
AA Mutation	p.Gln550His(p.Q550H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000273857
Start	47642047:47642047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2071A>T
AA Mutation	p.Thr691Ser(p.T691S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47595771:47595771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758207729
CDS Mutation	c.3079G>A
AA Mutation	p.Val1027Ile(p.V1027I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47645117:47645117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1921C>A
AA Mutation	p.Pro641Thr(p.P641T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47661778:47661778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1668T>G
AA Mutation	p.Asp556Glu(p.D556E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47680243:47680243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030C>T
AA Mutation	p.Pro344Ser(p.P344S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47763386:47763386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554037472
CDS Mutation	c.610G>A
AA Mutation	p.Asp204Asn(p.D204N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47763558:47763558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.438G>C
AA Mutation	p.Gln146His(p.Q146H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47786742:47786742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.392A>G
AA Mutation	p.Gln131Arg(p.Q131R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273857
Start	47626455:47626455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2265C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273857
Start	47692995:47692995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273857
Start	47692983:47692983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273857
Start	47786909:47786909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273857
Start	47603461:47603461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750625096
CDS Mutation	c.2748G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000273857
Start	47626520:47626520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2200G>T
AA Mutation	p.Glu734Ter(p.E734*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000273857
Start	47623666:47623666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2445G>A
AA Mutation	p.Trp815Ter(p.W815*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000273857
Start	47653552:47653552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1843+1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CORIN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47674426:47674426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1324C>G
AA Mutation	p.Leu442Val(p.L442V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47595779:47595779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3071C>T
AA Mutation	p.Ser1024Leu(p.S1024L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273857
Start	47680204:47680204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149671375
CDS Mutation	c.1069G>A
AA Mutation	p.Ala357Thr(p.A357T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273857
Start	47645163:47645163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1875A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273857
Start	47763431:47763431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.565C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000273857
Start	47623647:47623647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2464G>T
AA Mutation	p.Glu822Ter(p.E822*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000273857
Start	47626520:47626520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2200G>T
AA Mutation	p.Glu734Ter(p.E734*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript