Colon Cancer: Gene >> LRMP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354454
Start	25079436:25079436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753672679
CDS Mutation	c.110C>T
AA Mutation	p.Ser37Leu(p.S37L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354454
Start	25088104:25088104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776760281
CDS Mutation	c.320C>T
AA Mutation	p.Ala107Val(p.A107V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000354454
Start	25104362:25104362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769439544
CDS Mutation	c.1048C>T
AA Mutation	p.Arg350Cys(p.R350C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000354454
Start	25090185:25090185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594A>C
AA Mutation	p.Leu198Phe(p.L198F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000354454
Start	25107882:25107882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322T>C
AA Mutation	p.Leu441Pro(p.L441P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354454
Start	25079261:25079261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114104872
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354454
Start	25104368:25104368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1054T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354454
Start	25107042:25107042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1248C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354454
Start	25090110:25090110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354454
Start	25107898:25107898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1338A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000354454
Start	25090183:25090184(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.592_593insG
AA Mutation	p.Leu198CysfsTer12(p.L198Cfs*12)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LRMP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000354454
Start	25101310:25101310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874C>T
AA Mutation	p.Pro292Ser(p.P292S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000354454
Start	25079704:25079704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.185A>T
AA Mutation	p.Asn62Ile(p.N62I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354454
Start	25079443:25079443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.117C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000354454
Start	25108012:25108012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1452C>A
Mutation Classification	Silent
Feature Type	Transcript