Colon Cancer: Gene >> KLF17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372299
Start	44130516:44130516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930G>T
AA Mutation	p.Glu310Asp(p.E310D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372299
Start	44129803:44129803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773530149
CDS Mutation	c.532C>T
AA Mutation	p.Pro178Ser(p.P178S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372299
Start	44130608:44130608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141181356
CDS Mutation	c.1022G>A
AA Mutation	p.Arg341Gln(p.R341Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372299
Start	44130700:44130700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746750521
CDS Mutation	c.1114C>A
AA Mutation	p.Pro372Thr(p.P372T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372299
Start	44129504:44129504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377749405
CDS Mutation	c.233C>T
AA Mutation	p.Pro78Leu(p.P78L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372299
Start	44118932:44118932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.25A>G
AA Mutation	p.Met9Val(p.M9V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372299
Start	44118918:44118918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747380426
CDS Mutation	c.11G>A
AA Mutation	p.Arg4Gln(p.R4Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372299
Start	44130135:44130135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864G>T
AA Mutation	p.Glu288Asp(p.E288D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372299
Start	44118922:44118922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372299
Start	44118949:44118949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.42G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372299
Start	44129574:44129574(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.307delC
AA Mutation	p.Gln103LysfsTer9(p.Q103Kfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000372299
Start	44130670:44130670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1084C>T
AA Mutation	p.Gln362Ter(p.Q362*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KLF17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372299
Start	44130562:44130562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745641456
CDS Mutation	c.976C>T
AA Mutation	p.Arg326Cys(p.R326C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372299
Start	44129613:44129613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.342T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000372299
Start	44129390:44129390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.119C>A
AA Mutation	p.Ser40Ter(p.S40*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript