Colon Cancer: Gene >> STS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217961
Start	7350110:7350110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370888998
CDS Mutation	c.1601C>T
AA Mutation	p.Ala534Val(p.A534V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217961
Start	7334036:7334036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146965552
CDS Mutation	c.1307G>A
AA Mutation	p.Arg436His(p.R436H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217961
Start	7257358:7257358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.269G>A
AA Mutation	p.Arg90Gln(p.R90Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217961
Start	7259490:7259490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.539C>T
AA Mutation	p.Thr180Met(p.T180M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000217961
Start	7305182:7305182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1095A>T
AA Mutation	p.Lys365Asn(p.K365N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217961
Start	7259594:7259594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.643G>A
AA Mutation	p.Val215Ile(p.V215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000217961
Start	7275977:7275977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.848T>C
AA Mutation	p.Val283Ala(p.V283A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000217961
Start	7257258:7257258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760368070
CDS Mutation	c.169C>T
AA Mutation	p.Arg57Trp(p.R57W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000217961
Start	7253290:7253290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106G>A
AA Mutation	p.Asp36Asn(p.D36N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000217961
Start	7259615:7259615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.664C>A
AA Mutation	p.Leu222Ile(p.L222I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217961
Start	7349946:7349946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755417956
CDS Mutation	c.1437C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217961
Start	7349979:7349979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1470C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217961
Start	7305075:7305075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.988A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217961
Start	7259595:7259595(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.650delT
AA Mutation	p.Phe217SerfsTer6(p.F217Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217961
Start	7259515:7259515(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.568delC
AA Mutation	p.Leu190CysfsTer24(p.L190Cfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000217961
Start	7257288:7257288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199C>T
AA Mutation	p.Gln67Ter(p.Q67*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000217961
Start	7325337:7325337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> STS

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217961
Start	7349946:7349946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755417956
CDS Mutation	c.1437C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000217961
Start	7257589:7257589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.397+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript