Colon Cancer: Gene >> KSR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27607961:27607961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1697C>T
AA Mutation	p.Thr566Met(p.T566M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27582690:27582690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759278857
CDS Mutation	c.154C>T
AA Mutation	p.Arg52Trp(p.R52W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27605669:27605669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1505G>A
AA Mutation	p.Arg502His(p.R502H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27592579:27592579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Ala281Thr(p.A281T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27605744:27605744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1580C>T
AA Mutation	p.Thr527Met(p.T527M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27617389:27617389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2243G>A
AA Mutation	p.Arg748Gln(p.R748Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27601920:27601920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1127G>A
AA Mutation	p.Cys376Tyr(p.C376Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000398988
Start	27582648:27582648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112G>T
AA Mutation	p.Gly38Trp(p.G38W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27582988:27582988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746791967
CDS Mutation	c.452C>T
AA Mutation	p.Thr151Met(p.T151M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27607928:27607928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1664G>A
AA Mutation	p.Arg555Gln(p.R555Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27582777:27582777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241G>T
AA Mutation	p.Ala81Ser(p.A81S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000398988
Start	27582718:27582718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751430732
CDS Mutation	c.182C>T
AA Mutation	p.Thr61Met(p.T61M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398988
Start	27577611:27577611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398988
Start	27583091:27583091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376690107
CDS Mutation	c.555C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398988
Start	27605481:27605481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373150357
CDS Mutation	c.1317C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398988
Start	27592584:27592584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.846C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398988
Start	27588519:27588519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398988
Start	27604695:27604695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778827990
CDS Mutation	c.1236G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398988
Start	27582990:27582990(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs763290558
CDS Mutation	c.461delC
AA Mutation	p.Pro154HisfsTer36(p.P154Hfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KSR1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398988
Start	27607932:27607932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756639082
CDS Mutation	c.1668G>A
Mutation Classification	Silent
Feature Type	Transcript