Colon Cancer: Gene >> DCT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94462076:94462076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140917943
CDS Mutation	c.977G>A
AA Mutation	p.Arg326Gln(p.R326Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94443534:94443534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776332822
CDS Mutation	c.1283G>A
AA Mutation	p.Arg428Gln(p.R428Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94468878:94468878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762745612
CDS Mutation	c.463G>A
AA Mutation	p.Asp155Asn(p.D155N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94479164:94479164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375600704
CDS Mutation	c.92C>T
AA Mutation	p.Thr31Met(p.T31M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94479063:94479063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>G
AA Mutation	p.Arg65Gly(p.R65G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94479009:94479009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763411727
CDS Mutation	c.247C>T
AA Mutation	p.Arg83Cys(p.R83C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94439962:94439962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562777602
CDS Mutation	c.1496G>A
AA Mutation	p.Arg499Gln(p.R499Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94443445:94443445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1372G>A
AA Mutation	p.Asp458Asn(p.D458N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94479023:94479023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.233G>A
AA Mutation	p.Arg78Gln(p.R78Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377028
Start	94468912:94468912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755335828
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained;protein_altering_variant
Transcription ID	ENST00000377028
Start	94443558:94443559(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1258_1259insCAT
AA Mutation	p.Glu420delinsAlaTer(p.E420delinsA*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DCT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94468899:94468899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751146188
CDS Mutation	c.442G>A
AA Mutation	p.Ala148Thr(p.A148T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94466572:94466572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682G>A
AA Mutation	p.Glu228Lys(p.E228K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94460182:94460182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1088C>A
AA Mutation	p.Ser363Tyr(p.S363Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94466566:94466566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.688G>A
AA Mutation	p.Asp230Asn(p.D230N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377028
Start	94439904:94439904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1554A>C
AA Mutation	p.Glu518Asp(p.E518D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377028
Start	94460211:94460211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1059G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000377028
Start	94462077:94462077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148575940
CDS Mutation	c.976C>T
AA Mutation	p.Arg326Ter(p.R326*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000377028
Start	94439963:94439963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200349922
CDS Mutation	c.1495C>T
AA Mutation	p.Arg499Ter(p.R499*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript