Colon Cancer: Gene >> SHMT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328923
Start	57233614:57233614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1075C>T
AA Mutation	p.Arg359Trp(p.R359W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328923
Start	57233329:57233329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1007C>A
AA Mutation	p.Ala336Asp(p.A336D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328923
Start	57232221:57232221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>A
AA Mutation	p.Gly175Ser(p.G175S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328923
Start	57231508:57231508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373156028
CDS Mutation	c.259G>A
AA Mutation	p.Ala87Thr(p.A87T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328923
Start	57232560:57232560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561041442
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328923
Start	57232763:57232763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781224640
CDS Mutation	c.777G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328923
Start	57233300:57233300(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.982delC
AA Mutation	p.His328ThrfsTer8(p.H328Tfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SHMT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328923
Start	57232477:57232477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.619A>C
AA Mutation	p.Asn207His(p.N207H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328923
Start	57232268:57232268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.570C>T
Mutation Classification	Silent
Feature Type	Transcript