Colon Cancer: Gene >> CYP2A13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41089050:41089050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148044792
CDS Mutation	c.302G>A
AA Mutation	p.Arg101Gln(p.R101Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41093656:41093656(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858C>A
AA Mutation	p.Phe286Leu(p.F286L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41089007:41089007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753958154
CDS Mutation	c.259G>A
AA Mutation	p.Val87Ile(p.V87I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41091850:41091850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138089886
CDS Mutation	c.773C>T
AA Mutation	p.Thr258Met(p.T258M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000330436
Start	41093769:41093769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139418060
CDS Mutation	c.971A>G
AA Mutation	p.Glu324Gly(p.E324G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41088490:41088490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19C>A
AA Mutation	p.Leu7Ile(p.L7I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41095778:41095778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322G>A
AA Mutation	p.Gly441Glu(p.G441E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41090517:41090517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745929748
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Cys(p.R203C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41091811:41091811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.734A>C
AA Mutation	p.Glu245Ala(p.E245A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41090518:41090518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370968595
CDS Mutation	c.608G>A
AA Mutation	p.Arg203His(p.R203H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330436
Start	41088573:41088573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.102T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000330436
Start	41088536:41088536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65C>A
AA Mutation	p.Ser22Ter(p.S22*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2A13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41090479:41090479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.569G>A
AA Mutation	p.Arg190His(p.R190H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330436
Start	41088641:41088641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765068223
CDS Mutation	c.170C>T
AA Mutation	p.Ser57Phe(p.S57F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript