Colon Cancer: Gene >> GFAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253408
Start	44911398:44911398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.965C>T
AA Mutation	p.Ala322Val(p.A322V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253408
Start	44915473:44915473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773456179
CDS Mutation	c.14G>A
AA Mutation	p.Arg5His(p.R5H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253408
Start	44913360:44913360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.689A>G
AA Mutation	p.Asp230Gly(p.D230G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253408
Start	44913319:44913319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>A
AA Mutation	p.Ala244Thr(p.A244T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253408
Start	44908138:44908138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183G>A
AA Mutation	p.Asp395Asn(p.D395N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253408
Start	44915199:44915199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.288G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253408
Start	44915381:44915381(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.106delC
AA Mutation	p.Arg36AlafsTer38(p.R36Afs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GFAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253408
Start	44913289:44913289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745784904
CDS Mutation	c.760G>A
AA Mutation	p.Glu254Lys(p.E254K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253408
Start	44915199:44915199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779815330
CDS Mutation	c.288G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253408
Start	44908115:44908115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1206C>A
Mutation Classification	Silent
Feature Type	Transcript