Colon Cancer: Gene >> CERS3

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000284382
Start	100472926:100472926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736G>A
AA Mutation	p.Glu246Lys(p.E246K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100480041:100480041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.413G>A
AA Mutation	p.Arg138Lys(p.R138K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100490881:100490881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Arg75Gln(p.R75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100472941:100472941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.721G>A
AA Mutation	p.Ala241Thr(p.A241T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100469399:100469399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143625266
CDS Mutation	c.824G>A
AA Mutation	p.Arg275His(p.R275H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100484634:100484634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323T>C
AA Mutation	p.Leu108Ser(p.L108S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100484631:100484631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138661052
CDS Mutation	c.326C>T
AA Mutation	p.Thr109Met(p.T109M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100455942:100455942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950A>G
AA Mutation	p.Tyr317Cys(p.Y317C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100501759:100501759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.91C>T
AA Mutation	p.Leu31Phe(p.L31F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100455904:100455904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988A>G
AA Mutation	p.Ile330Val(p.I330V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284382
Start	100469443:100469443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.780T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284382
Start	100402812:100402812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1053G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000284382
Start	100402764:100402764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs556349640
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CERS3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100456032:100456032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771534407
CDS Mutation	c.860C>T
AA Mutation	p.Thr287Met(p.T287M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100501756:100501756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142269983
CDS Mutation	c.94G>A
AA Mutation	p.Val32Ile(p.V32I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100476092:100476092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603G>T
AA Mutation	p.Lys201Asn(p.K201N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100490853:100490853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.252G>T
AA Mutation	p.Glu84Asp(p.E84D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100484637:100484637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.320A>G
AA Mutation	p.Asn107Ser(p.N107S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100402817:100402817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1048G>A
AA Mutation	p.Glu350Lys(p.E350K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000284382
Start	100472977:100472977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Cys(p.R229C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000284382
Start	100501831:100501831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19G>T
AA Mutation	p.Glu7Ter(p.E7*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript