Colon Cancer: Gene >> SLC43A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000278426
Start	57488958:57488958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1367G>A
AA Mutation	p.Arg456Gln(p.R456Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000278426
Start	57500846:57500846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202015221
CDS Mutation	c.398C>T
AA Mutation	p.Pro133Leu(p.P133L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000278426
Start	57496055:57496055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668C>A
AA Mutation	p.Pro223His(p.P223H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000278426
Start	57489350:57489350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1236G>T
AA Mutation	p.Lys412Asn(p.K412N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000278426
Start	57496155:57496155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200711356
CDS Mutation	c.568G>A
AA Mutation	p.Asp190Asn(p.D190N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278426
Start	57491804:57491804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000278426
Start	57501214:57501214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC43A1

No Mutation Annotation!