Colon Cancer: Gene >> SHMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316694
Start	18340162:18340162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.695T>C
AA Mutation	p.Ile232Thr(p.I232T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316694
Start	18330663:18330663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063G>T
AA Mutation	p.Asp355Tyr(p.D355Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316694
Start	18340765:18340765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.568G>A
AA Mutation	p.Ala190Thr(p.A190T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316694
Start	18353777:18353777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137T>C
AA Mutation	p.Val46Ala(p.V46A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316694
Start	18329356:18329356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1204C>T
AA Mutation	p.Arg402Trp(p.R402W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316694
Start	18340193:18340193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530339034
CDS Mutation	c.664G>A
AA Mutation	p.Gly222Arg(p.G222R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316694
Start	18329334:18329334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150725254
CDS Mutation	c.1226C>T
AA Mutation	p.Thr409Met(p.T409M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316694
Start	18329333:18329333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1227G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316694
Start	18347583:18347583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151202813
CDS Mutation	c.432G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316694
Start	18347577:18347577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000316694
Start	18347575:18347575(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.440delG
AA Mutation	p.Gly147AlafsTer3(p.G147Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000316694
Start	18353739:18353739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570376791
CDS Mutation	c.175C>T
AA Mutation	p.Arg59Ter(p.R59*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SHMT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316694
Start	18330627:18330627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1099G>T
AA Mutation	p.Gly367Cys(p.G367C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript