Colon Cancer: Gene >> SLC22A12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377574
Start	64591622:64591622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.66G>A
AA Mutation	p.Met22Ile(p.M22I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377574
Start	64593466:64593466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568G>A
AA Mutation	p.Ala190Thr(p.A190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377574
Start	64599852:64599852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1247C>T
AA Mutation	p.Ala416Val(p.A416V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377574
Start	64600453:64600453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747742344
CDS Mutation	c.1372G>A
AA Mutation	p.Glu458Lys(p.E458K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377574
Start	64598517:64598517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832T>C
AA Mutation	p.Trp278Arg(p.W278R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377574
Start	64593534:64593534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377574
Start	64592862:64592862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376212424
CDS Mutation	c.486G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377574
Start	64600756:64600756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1416C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377574
Start	64599802:64599802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1197G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377574
Start	64593762:64593762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.789G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377574
Start	64593516:64593516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377574
Start	64593702:64593702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750178384
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377574
Start	64592787:64592787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377574
Start	64599883:64599884(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1282dupC
AA Mutation	p.His428ProfsTer178(p.H428Pfs*178)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377574
Start	64593686:64593686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713C>A
AA Mutation	p.Ser238Tyr(p.S238Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript