Colon Cancer: Gene >> DGKG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265022
Start	186279937:186279937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200662645
CDS Mutation	c.706C>T
AA Mutation	p.Arg236Trp(p.R236W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265022
Start	186260484:186260484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1379A>G
AA Mutation	p.Asn460Ser(p.N460S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265022
Start	186164950:186164950(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2164G>T
AA Mutation	p.Gly722Cys(p.G722C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265022
Start	186251845:186251845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1675C>T
AA Mutation	p.His559Tyr(p.H559Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265022
Start	186260506:186260506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373512874
CDS Mutation	c.1357C>T
AA Mutation	p.Arg453Trp(p.R453W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265022
Start	186211879:186211879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1833G>T
AA Mutation	p.Lys611Asn(p.K611N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000265022
Start	186272306:186272306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948A>C
AA Mutation	p.Arg316Ser(p.R316S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000265022
Start	186272320:186272320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199698541
CDS Mutation	c.934C>T
AA Mutation	p.Arg312Cys(p.R312C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265022
Start	186284678:186284678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768853121
CDS Mutation	c.576C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265022
Start	186188239:186188239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2058T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265022
Start	186267742:186267742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770406720
CDS Mutation	c.1152C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265022
Start	186188278:186188278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2019C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265022
Start	186164969:186164969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2145G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265022
Start	186288824:186288824(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.430delC
AA Mutation	p.Leu144TrpfsTer18(p.L144Wfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000265022
Start	186188308:186188308(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1989delG
AA Mutation	p.Met663IlefsTer17(p.M663Ifs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DGKG

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265022
Start	186298101:186298101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778226991
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265022
Start	186288792:186288792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758220917
CDS Mutation	c.462G>A
Mutation Classification	Silent
Feature Type	Transcript