Colon Cancer: Gene >> LPIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11804450:11804450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1933A>G
AA Mutation	p.Asn645Asp(p.N645D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11783841:11783841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747610587
CDS Mutation	c.1169G>A
AA Mutation	p.Arg390Gln(p.R390Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11771487:11771487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757466722
CDS Mutation	c.404C>T
AA Mutation	p.Thr135Met(p.T135M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11771394:11771394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311C>T
AA Mutation	p.Ala104Val(p.A104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11804495:11804495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778277029
CDS Mutation	c.1978C>T
AA Mutation	p.Arg660Cys(p.R660C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11784905:11784905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746840869
CDS Mutation	c.1270G>A
AA Mutation	p.Ala424Thr(p.A424T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11783862:11783862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190T>C
AA Mutation	p.Val397Ala(p.V397A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11819561:11819561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2372C>T
AA Mutation	p.Thr791Ile(p.T791I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256720
Start	11804452:11804452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372109726
CDS Mutation	c.1935C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256720
Start	11771512:11771512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145629147
CDS Mutation	c.429C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256720
Start	11771647:11771647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149765431
CDS Mutation	c.564G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256720
Start	11782317:11782317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368925424
CDS Mutation	c.966G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000256720
Start	11771425:11771426(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.342_343insTTAATTC
AA Mutation	p.Arg115LeufsTer59(p.R115Lfs*59)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LPIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11819499:11819499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2310G>T
AA Mutation	p.Lys770Asn(p.K770N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11784920:11784920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285G>A
AA Mutation	p.Asp429Asn(p.D429N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000256720
Start	11767850:11767850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.280A>C
AA Mutation	p.Asn94His(p.N94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000256720
Start	11820479:11820479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2478G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000256720
Start	11767772:11767772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>T
AA Mutation	p.Glu68Ter(p.E68*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000256720
Start	11820429:11820429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2428C>T
AA Mutation	p.Gln810Ter(p.Q810*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000256720
Start	11791913:11791913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1606-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript