Colon Cancer: Gene >> LCAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264005
Start	67944083:67944083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19C>T
AA Mutation	p.Pro7Ser(p.P7S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264005
Start	67944085:67944085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.17C>T
AA Mutation	p.Ser6Phe(p.S6F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264005
Start	67942548:67942548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563T>C
AA Mutation	p.Val188Ala(p.V188A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264005
Start	67940238:67940238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989C>T
AA Mutation	p.Ala330Val(p.A330V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264005
Start	67940100:67940100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1127G>T
AA Mutation	p.Ser376Ile(p.S376I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264005
Start	67940165:67940165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1062C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264005
Start	67943991:67943991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.111G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264005
Start	67942940:67942940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747530363
CDS Mutation	c.348C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264005
Start	67944001:67944001(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.101delC
AA Mutation	p.Pro34ArgfsTer27(p.P34Rfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264005
Start	67944030:67944030(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.72delC
AA Mutation	p.Phe25SerfsTer36(p.F25Sfs*36)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LCAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264005
Start	67940257:67940257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.970C>A
AA Mutation	p.Leu324Ile(p.L324I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264005
Start	67944090:67944090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.12C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264005
Start	67942511:67942511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753143565
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript