Colon Cancer: Gene >> CYP7A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58492510:58492510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778961537
CDS Mutation	c.1058C>T
AA Mutation	p.Ser353Leu(p.S353L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58496820:58496820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780668040
CDS Mutation	c.692C>T
AA Mutation	p.Ala231Val(p.A231V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58492423:58492423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772557610
CDS Mutation	c.1145G>A
AA Mutation	p.Arg382Gln(p.R382Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58496671:58496671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841G>A
AA Mutation	p.Val281Met(p.V281M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58498344:58498344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206G>A
AA Mutation	p.Cys69Tyr(p.C69Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58497061:58497061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451C>T
AA Mutation	p.Arg151Cys(p.R151C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58496814:58496814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs8192874
CDS Mutation	c.698A>G
AA Mutation	p.Asn233Ser(p.N233S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58496876:58496876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.636C>A
AA Mutation	p.Phe212Leu(p.F212L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58496848:58496848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664G>C
AA Mutation	p.Gly222Arg(p.G222R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58491510:58491510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1480G>T
AA Mutation	p.Asp494Tyr(p.D494Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000301645
Start	58496982:58496982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.530G>T
AA Mutation	p.Arg177Leu(p.R177L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301645
Start	58491648:58491648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1342T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301645
Start	58496810:58496810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.702C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant;start_lost
Transcription ID	ENST00000301645
Start	58500098:58500098(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1delA
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301645
Start	58498316:58498317(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.233dupT
AA Mutation	p.Ile79HisfsTer9(p.I79Hfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CYP7A1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301645
Start	58496876:58496876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370087640
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301645
Start	58494627:58494627(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.918delA
AA Mutation	p.Ala307GlnfsTer2(p.A307Qfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript