Colon Cancer: Gene >> SLC37A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352133
Start	42518502:42518502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.48G>T
AA Mutation	p.Arg16Ser(p.R16S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000352133
Start	42547106:42547106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.734C>T
AA Mutation	p.Pro245Leu(p.P245L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000352133
Start	42574830:42574830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436G>C
AA Mutation	p.Gly479Ala(p.G479A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000352133
Start	42525835:42525835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771532998
CDS Mutation	c.116G>A
AA Mutation	p.Arg39Gln(p.R39Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000352133
Start	42518479:42518479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546388927
CDS Mutation	c.25C>T
AA Mutation	p.Arg9Cys(p.R9C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000352133
Start	42564720:42564720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1148C>T
AA Mutation	p.Ala383Val(p.A383V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352133
Start	42539584:42539584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.423C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000352133
Start	42539572:42539572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573347357
CDS Mutation	c.411C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352133
Start	42563829:42563829(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1091delA
AA Mutation	p.Lys364ArgfsTer22(p.K364Rfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352133
Start	42562112:42562112(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1017delC
AA Mutation	p.Lys340SerfsTer46(p.K340Sfs*46)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000352133
Start	42534779:42534780(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.226dupC
AA Mutation	p.His76ProfsTer5(p.H76Pfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SLC37A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000352133
Start	42568427:42568427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771928444
CDS Mutation	c.1412C>T
AA Mutation	p.Thr471Met(p.T471M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript