Colon Cancer: Gene >> SLC22A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377871
Start	62981052:62981052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.970G>T
AA Mutation	p.Ala324Ser(p.A324S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377871
Start	62981872:62981872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11568624
CDS Mutation	c.767C>T
AA Mutation	p.Ala256Val(p.A256V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377871
Start	62984606:62984606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.85C>T
AA Mutation	p.Leu29Phe(p.L29F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377871
Start	62977205:62977205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372804378
CDS Mutation	c.1544C>T
AA Mutation	p.Thr515Met(p.T515M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377871
Start	62984404:62984404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287C>G
AA Mutation	p.Ala96Gly(p.A96G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377871
Start	62983620:62983620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.545C>T
AA Mutation	p.Ala182Val(p.A182V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377871
Start	62979883:62979883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1103A>G
AA Mutation	p.Tyr368Cys(p.Y368C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377871
Start	62984453:62984453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238C>T
AA Mutation	p.Arg80Cys(p.R80C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377871
Start	62979867:62979867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1119C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377871
Start	62977183:62977183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1566G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377871
Start	62984376:62984376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.315C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377871
Start	62983598:62983598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747211281
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377871
Start	62981862:62981862(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769180324
CDS Mutation	c.777delT
AA Mutation	p.Phe259LeufsTer27(p.F259Lfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC22A6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377871
Start	62981897:62981897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760972754
CDS Mutation	c.742C>T
AA Mutation	p.Arg248Cys(p.R248C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377871
Start	62979529:62979529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766774811
CDS Mutation	c.1320C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377871
Start	62983961:62983961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769299835
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript