Colon Cancer: Gene >> SLC36A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243389
Start	151458877:151458877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85C>A
AA Mutation	p.Leu29Ile(p.L29I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243389
Start	151488007:151488007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749715139
CDS Mutation	c.1184G>A
AA Mutation	p.Arg395His(p.R395H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243389
Start	151479387:151479387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781266508
CDS Mutation	c.1057G>A
AA Mutation	p.Val353Ile(p.V353I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243389
Start	151479432:151479432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751677534
CDS Mutation	c.1102G>A
AA Mutation	p.Glu368Lys(p.E368K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000243389
Start	151479372:151479372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758625230
CDS Mutation	c.1042G>A
AA Mutation	p.Ala348Thr(p.A348T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000243389
Start	151464536:151464536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.257T>G
AA Mutation	p.Ile86Ser(p.I86S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000243389
Start	151467923:151467923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721C>G
AA Mutation	p.Gln241Glu(p.Q241E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000243389
Start	151467924:151467924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.722A>T
AA Mutation	p.Gln241Leu(p.Q241L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000243389
Start	151467821:151467821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619C>A
AA Mutation	p.Leu207Met(p.L207M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243389
Start	151467718:151467718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751904883
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243389
Start	151488023:151488023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373317838
CDS Mutation	c.1200C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243389
Start	151488050:151488050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148310645
CDS Mutation	c.1227C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000243389
Start	151467785:151467785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.583C>T
AA Mutation	p.Arg195Ter(p.R195*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC36A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243389
Start	151464598:151464598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142033033
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Cys(p.R107C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript