Colon Cancer: Gene >> EFNB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000204961
Start	68840035:68840035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575C>T
AA Mutation	p.Ala192Val(p.A192V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000204961
Start	68840533:68840533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920G>A
AA Mutation	p.Arg307Gln(p.R307Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000204961
Start	68838700:68838700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767055938
CDS Mutation	c.212G>A
AA Mutation	p.Arg71Gln(p.R71Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000204961
Start	68838699:68838699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367996552
CDS Mutation	c.211C>T
AA Mutation	p.Arg71Trp(p.R71W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000204961
Start	68840371:68840371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758T>A
AA Mutation	p.Leu253His(p.L253H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000204961
Start	68838857:68838857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000204961
Start	68840320:68840327(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.707_714delCCAAGGTG
AA Mutation	p.Ser236CysfsTer80(p.S236Cfs*80)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000204961
Start	68840480:68840480(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.872delG
AA Mutation	p.Gly291AlafsTer30(p.G291Afs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000204961
Start	68838887:68838887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.399C>A
AA Mutation	p.Tyr133Ter(p.Y133*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000204961
Start	68840369:68840370(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.756_757insGTT
AA Mutation	p.Leu252_Leu253insVal(p.L252_L253insV)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EFNB1

No Mutation Annotation!