Colon Cancer: Gene >> AHR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17339330:17339330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533269895
CDS Mutation	c.1505C>T
AA Mutation	p.Pro502Leu(p.P502L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17334892:17334892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769847453
CDS Mutation	c.914G>A
AA Mutation	p.Arg305Lys(p.R305K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17322598:17322598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351C>A
AA Mutation	p.Phe117Leu(p.F117L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17309998:17309998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.128T>C
AA Mutation	p.Leu43Pro(p.L43P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17339298:17339298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1473T>A
AA Mutation	p.Asn491Lys(p.N491K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17322533:17322533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766592204
CDS Mutation	c.286G>A
AA Mutation	p.Gly96Arg(p.G96R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17339204:17339204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1379T>G
AA Mutation	p.Met460Arg(p.M460R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17339335:17339335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1510G>A
AA Mutation	p.Gly504Arg(p.G504R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17338997:17338997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1172G>T
AA Mutation	p.Gly391Val(p.G391V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17310090:17310090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545782208
CDS Mutation	c.220G>A
AA Mutation	p.Val74Ile(p.V74I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242057
Start	17310089:17310089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761236007
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242057
Start	17339001:17339001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1176A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242057
Start	17339737:17339737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1912C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242057
Start	17340075:17340075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2250T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242057
Start	17339631:17339631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1806A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242057
Start	17330838:17330838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242057
Start	17339471:17339474(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1646_1649delATTT
AA Mutation	p.Asp549ValfsTer28(p.D549Vfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242057
Start	17339506:17339506(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1685delT
AA Mutation	p.Phe562SerfsTer16(p.F562Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AHR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17339018:17339018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193G>A
AA Mutation	p.Arg398Gln(p.R398Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17330015:17330015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Cys(p.R172C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17340034:17340034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2209G>T
AA Mutation	p.Asp737Tyr(p.D737Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242057
Start	17339158:17339158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333A>G
AA Mutation	p.Thr445Ala(p.T445A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242057
Start	17339025:17339025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201080105
CDS Mutation	c.1200G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242057
Start	17343016:17343016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763058807
CDS Mutation	c.2499G>A
Mutation Classification	Silent
Feature Type	Transcript