Colon Cancer: Gene >> SHBG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380450
Start	7631703:7631703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670G>A
AA Mutation	p.Gly224Arg(p.G224R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380450
Start	7630199:7630199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380450
Start	7630247:7630247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380450
Start	7630202:7630202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201603103
CDS Mutation	c.30G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380450
Start	7631323:7631323(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.522delG
AA Mutation	p.Leu175CysfsTer45(p.L175Cfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380450
Start	7633223:7633223(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1084delT
AA Mutation	p.Cys362AlafsTer2(p.C362Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000380450
Start	7631322:7631323(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.522dupG
AA Mutation	p.Leu175AlafsTer39(p.L175Afs*39)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SHBG

No Mutation Annotation!