Colon Cancer: Gene >> SLCO4C1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102240748:102240748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1846G>A
AA Mutation	p.Gly616Arg(p.G616R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102239301:102239301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1964C>A
AA Mutation	p.Ala655Asp(p.A655D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102239271:102239271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1994C>T
AA Mutation	p.Ala665Val(p.A665V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102270677:102270677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769468689
CDS Mutation	c.749G>A
AA Mutation	p.Gly250Glu(p.G250E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102296134:102296134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129T>G
AA Mutation	p.Asn43Lys(p.N43K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102247360:102247360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1703G>T
AA Mutation	p.Gly568Val(p.G568V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102296042:102296042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.221A>C
AA Mutation	p.Lys74Thr(p.K74T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102257242:102257242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1342A>G
AA Mutation	p.Met448Val(p.M448V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102262013:102262013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.920A>T
AA Mutation	p.Asp307Val(p.D307V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102291406:102291406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556G>A
AA Mutation	p.Ala186Thr(p.A186T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102249735:102249735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529284686
CDS Mutation	c.1523C>T
AA Mutation	p.Ser508Leu(p.S508L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102247339:102247339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144643168
CDS Mutation	c.1724C>T
AA Mutation	p.Ala575Val(p.A575V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310954
Start	102257147:102257147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1437G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310954
Start	102263718:102263718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.865C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310954
Start	102239327:102239327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1938T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310954
Start	102258043:102258043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1173T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000310954
Start	102249733:102249733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754562682
CDS Mutation	c.1525C>T
AA Mutation	p.Arg509Ter(p.R509*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLCO4C1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310954
Start	102296232:102296232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>A
AA Mutation	p.Ala11Thr(p.A11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310954
Start	102296167:102296167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.96C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310954
Start	102291392:102291392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.570A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000310954
Start	102236983:102236983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2050G>T
AA Mutation	p.Gly684Ter(p.G684*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000310954
Start	102240727:102240727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202120876
CDS Mutation	c.1867C>T
AA Mutation	p.Arg623Ter(p.R623*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript