Colon Cancer: Gene >> SLC44A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105362852:105362852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368894258
CDS Mutation	c.932G>A
AA Mutation	p.Arg311His(p.R311H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105365539:105365539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540159903
CDS Mutation	c.1310G>A
AA Mutation	p.Arg437His(p.R437H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105364606:105364606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1139C>A
AA Mutation	p.Pro380His(p.P380H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105356250:105356250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539A>G
AA Mutation	p.Asn180Ser(p.N180S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105365599:105365599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1370G>A
AA Mutation	p.Arg457Gln(p.R457Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105362851:105362851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Cys(p.R311C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105362905:105362905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985A>G
AA Mutation	p.Ile329Val(p.I329V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105362933:105362933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1013C>T
AA Mutation	p.Pro338Leu(p.P338L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105366400:105366400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465C>A
AA Mutation	p.Leu489Ile(p.L489I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105309803:105309803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206G>A
AA Mutation	p.Cys69Tyr(p.C69Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105356338:105356338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761961178
CDS Mutation	c.627G>A
AA Mutation	p.Met209Ile(p.M209I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374720
Start	105348416:105348416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374720
Start	105385499:105385499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560665933
CDS Mutation	c.1947G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374720
Start	105309771:105309771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751129497
CDS Mutation	c.174A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC44A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105309767:105309767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.170G>T
AA Mutation	p.Arg57Ile(p.R57I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374720
Start	105335636:105335636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343G>A
AA Mutation	p.Ala115Thr(p.A115T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript