Colon Cancer: Gene >> L3MBTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43514701:43514701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361C>T
AA Mutation	p.Arg121Trp(p.R121W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43534873:43534873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766968999
CDS Mutation	c.1690G>A
AA Mutation	p.Ala564Thr(p.A564T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43536182:43536182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1945G>A
AA Mutation	p.Ala649Thr(p.A649T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43514744:43514744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.404C>T
AA Mutation	p.Ala135Val(p.A135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43540288:43540288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2245G>A
AA Mutation	p.Ala749Thr(p.A749T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43535843:43535843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1766G>T
AA Mutation	p.Arg589Ile(p.R589I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43534336:43534336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1586G>T
AA Mutation	p.Arg529Met(p.R529M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43534083:43534083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523C>T
AA Mutation	p.Ala508Val(p.A508V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418998
Start	43532862:43532862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576853992
CDS Mutation	c.1308C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418998
Start	43515103:43515103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418998
Start	43540812:43540812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377279389
CDS Mutation	c.2325C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418998
Start	43515088:43515088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562382937
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418998
Start	43515139:43515139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418998
Start	43540254:43540254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2211G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000418998
Start	43515049:43515049(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.482delC
AA Mutation	p.Pro161GlnfsTer39(p.P161Qfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> L3MBTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43540786:43540786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2299G>C
AA Mutation	p.Glu767Gln(p.E767Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000418998
Start	43536290:43536290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2053G>A
AA Mutation	p.Gly685Ser(p.G685S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000418998
Start	43529338:43529338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371655802
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript