Colon Cancer: Gene >> TGFB1I1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000394863
Start	31473837:31473837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201803234
CDS Mutation	c.185C>T
AA Mutation	p.Thr62Met(p.T62M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394863
Start	31473901:31473901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753388681
CDS Mutation	c.249C>A
AA Mutation	p.Ser83Arg(p.S83R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394863
Start	31473902:31473902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199836545
CDS Mutation	c.250G>A
AA Mutation	p.Gly84Ser(p.G84S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394863
Start	31474164:31474164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.338C>A
AA Mutation	p.Ser113Tyr(p.S113Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394863
Start	31477372:31477372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>T
AA Mutation	p.Glu394Asp(p.E394D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000394863
Start	31476099:31476099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.802G>A
AA Mutation	p.Glu268Lys(p.E268K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000394863
Start	31474747:31474747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.704T>A
AA Mutation	p.Ile235Asn(p.I235N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394863
Start	31473913:31473913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394863
Start	31473466:31473466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753968189
CDS Mutation	c.39T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394863
Start	31473711:31473711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000394863
Start	31474200:31474202(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.376_378delAAG
AA Mutation	p.Lys126del(p.K126del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TGFB1I1

No Mutation Annotation!