Colon Cancer: Gene >> TCF7L1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000282111
Start	85305340:85305340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.926C>A
AA Mutation	p.Ala309Asp(p.A309D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000282111
Start	85134343:85134343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.334G>A
AA Mutation	p.Ala112Thr(p.A112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000282111
Start	85302512:85302512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749872975
CDS Mutation	c.554C>T
AA Mutation	p.Pro185Leu(p.P185L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000282111
Start	85134436:85134436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427G>A
AA Mutation	p.Gly143Arg(p.G143R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000282111
Start	85305315:85305315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753284958
CDS Mutation	c.901C>T
AA Mutation	p.Pro301Ser(p.P301S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282111
Start	85133885:85133885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282111
Start	85309306:85309306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1611C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000282111
Start	85306475:85306475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1173A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282111
Start	85302566:85302566(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.612delC
AA Mutation	p.Gly205AlafsTer72(p.G205Afs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000282111
Start	85305375:85305375(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.966delC
AA Mutation	p.Ser323AlafsTer2(p.S323Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TCF7L1

No Mutation Annotation!