Colon Cancer: Gene >> MLIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54230742:54230742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375482204
CDS Mutation	c.1142C>T
AA Mutation	p.Ser381Leu(p.S381L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54121576:54121576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761764090
CDS Mutation	c.193G>A
AA Mutation	p.Asp65Asn(p.D65N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54121544:54121544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161A>C
AA Mutation	p.Lys54Thr(p.K54T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54149124:54149124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.681G>T
AA Mutation	p.Gln227His(p.Q227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54230883:54230883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283C>A
AA Mutation	p.Ser428Tyr(p.S428Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54124780:54124780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369010969
CDS Mutation	c.527G>A
AA Mutation	p.Arg176His(p.R176H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274897
Start	54160772:54160772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.867G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274897
Start	54124721:54124721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746829040
CDS Mutation	c.468C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274897
Start	54230872:54230872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1272A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000274897
Start	54149088:54149088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.645T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274897
Start	54124707:54124707(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.459delG
AA Mutation	p.Ile154LeufsTer11(p.I154Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274897
Start	54124700:54124700(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.452delC
AA Mutation	p.Pro151GlnfsTer14(p.P151Qfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000274897
Start	54202155:54202156(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1041dupA
AA Mutation	p.Glu348ArgfsTer6(p.E348Rfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MLIP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000274897
Start	54160753:54160753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848C>A
AA Mutation	p.Ser283Tyr(p.S283Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript