Colon Cancer: Gene >> LRRC28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301981
Start	99256011:99256011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54G>T
AA Mutation	p.Lys18Asn(p.K18N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301981
Start	99334034:99334034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375152645
CDS Mutation	c.497G>A
AA Mutation	p.Arg166Gln(p.R166Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301981
Start	99361437:99361437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797A>C
AA Mutation	p.Glu266Ala(p.E266A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301981
Start	99334057:99334057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769522349
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Cys(p.R174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301981
Start	99361382:99361382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.742T>G
AA Mutation	p.Ser248Ala(p.S248A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301981
Start	99334039:99334039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753306548
CDS Mutation	c.502C>T
AA Mutation	p.Arg168Cys(p.R168C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000301981
Start	99287814:99287814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248C>T
AA Mutation	p.Ala83Val(p.A83V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000301981
Start	99352414:99352414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.638A>G
AA Mutation	p.Asn213Ser(p.N213S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301981
Start	99352427:99352427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.651A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301981
Start	99287942:99287943(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.376_377insAAGTTAAAATATT
AA Mutation	p.Leu126GlnfsTer63(p.L126Qfs*63)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LRRC28

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301981
Start	99386069:99386069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript