Colon Cancer: Gene >> LPIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2921623:2921623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2352G>T
AA Mutation	p.Glu784Asp(p.E784D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2937821:2937821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1039G>A
AA Mutation	p.Glu347Lys(p.E347K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2925364:2925364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1798G>A
AA Mutation	p.Ala600Thr(p.A600T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2924438:2924438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2047G>A
AA Mutation	p.Asp683Asn(p.D683N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2951227:2951227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751024451
CDS Mutation	c.418G>A
AA Mutation	p.Val140Ile(p.V140I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2921590:2921590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2385G>T
AA Mutation	p.Lys795Asn(p.K795N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261596
Start	2960787:2960787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.54C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261596
Start	2925365:2925365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772568696
CDS Mutation	c.1797G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261596
Start	2960697:2960697(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.144delT
AA Mutation	p.His49ThrfsTer10(p.H49Tfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261596
Start	2924502:2924503(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1982_1983insC
AA Mutation	p.Ile662TyrfsTer22(p.I662Yfs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LPIN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2929126:2929126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201325845
CDS Mutation	c.1489G>A
AA Mutation	p.Glu497Lys(p.E497K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2951193:2951193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452C>A
AA Mutation	p.Ser151Tyr(p.S151Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2921590:2921590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2385G>T
AA Mutation	p.Lys795Asn(p.K795N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261596
Start	2923836:2923836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2113C>T
AA Mutation	p.Pro705Ser(p.P705S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript