Colon Cancer: Gene >> SLC11A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218394754:218394754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1511C>T
AA Mutation	p.Ala504Val(p.A504V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218389997:218389997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923A>C
AA Mutation	p.Gln308Pro(p.Q308P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218384312:218384312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.220G>A
AA Mutation	p.Asp74Asn(p.D74N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218394982:218394982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1600C>T
AA Mutation	p.His534Tyr(p.H534Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218384282:218384282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190C>G
AA Mutation	p.Pro64Ala(p.P64A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218386641:218386641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201910426
CDS Mutation	c.400C>T
AA Mutation	p.Arg134Cys(p.R134C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218387942:218387942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751137810
CDS Mutation	c.782C>T
AA Mutation	p.Ser261Leu(p.S261L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218393011:218393011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140431789
CDS Mutation	c.1195G>A
AA Mutation	p.Ala399Thr(p.A399T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218384259:218384259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167G>T
AA Mutation	p.Arg56Leu(p.R56L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233202
Start	218389998:218389998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.924G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000233202
Start	218387584:218387584(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.597delT
AA Mutation	p.Phe199LeufsTer5(p.F199Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SLC11A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218394949:218394949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142604013
CDS Mutation	c.1567G>A
AA Mutation	p.Gly523Arg(p.G523R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233202
Start	218394126:218394126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321T>C
AA Mutation	p.Phe441Leu(p.F441L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript