Colon Cancer: Gene >> GRB7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309156
Start	39743432:39743432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560775365
CDS Mutation	c.625G>A
AA Mutation	p.Asp209Asn(p.D209N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309156
Start	39742324:39742324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767188773
CDS Mutation	c.23C>T
AA Mutation	p.Pro8Leu(p.P8L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309156
Start	39744604:39744604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767271125
CDS Mutation	c.853G>A
AA Mutation	p.Val285Met(p.V285M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309156
Start	39743431:39743431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545599174
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309156
Start	39744621:39744621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309156
Start	39742663:39742663(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.257delG
AA Mutation	p.Gly86AlafsTer18(p.G86Afs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000309156
Start	39742692:39742692(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.286delC
AA Mutation	p.Arg96AlafsTer8(p.R96Afs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000309156
Start	39744940:39744940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.967G>T
AA Mutation	p.Glu323Ter(p.E323*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000309156
Start	39744898:39744898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.925C>T
AA Mutation	p.Arg309Ter(p.R309*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> GRB7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309156
Start	39743191:39743191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475G>A
AA Mutation	p.Glu159Lys(p.E159K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309156
Start	39746168:39746168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1418A>C
AA Mutation	p.His473Pro(p.H473P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000309156
Start	39742573:39742573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.163C>T
AA Mutation	p.Arg55Ter(p.R55*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript