Colon Cancer: Gene >> EFNB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226091
Start	7708032:7708032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370940378
CDS Mutation	c.197G>A
AA Mutation	p.Arg66Gln(p.R66Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226091
Start	7708200:7708200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.365C>A
AA Mutation	p.Pro122His(p.P122H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226091
Start	7708059:7708059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224A>T
AA Mutation	p.Asn75Ile(p.N75I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226091
Start	7708203:7708203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368A>C
AA Mutation	p.Asn123Thr(p.N123T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226091
Start	7708704:7708704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578C>A
AA Mutation	p.Ala193Asp(p.A193D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226091
Start	7709450:7709450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226091
Start	7709384:7709384(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.836delG
AA Mutation	p.Gly279ValfsTer15(p.G279Vfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226091
Start	7709538:7709538(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.991delC
AA Mutation	p.Gln331ArgfsTer39(p.Q331Rfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226091
Start	7708088:7708088(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.257delG
AA Mutation	p.Gly86ValfsTer72(p.G86Vfs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000226091
Start	7708515:7708515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496C>T
AA Mutation	p.Arg166Ter(p.R166*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226091
Start	7705621:7705622(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.29dupG
AA Mutation	p.Val11ArgfsTer30(p.V11Rfs*30)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226091
Start	7705604:7705605(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs745309220
CDS Mutation	c.13dupC
AA Mutation	p.His5ProfsTer36(p.H5Pfs*36)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226091
Start	7709537:7709538(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs756422375
CDS Mutation	c.991dupC
AA Mutation	p.Gln331ProfsTer20(p.Q331Pfs*20)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EFNB3

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000226091
Start	7709538:7709538(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.991delC
AA Mutation	p.Gln331ArgfsTer39(p.Q331Rfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript