Colon Cancer: Gene >> LDLR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11100246:11100246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776421777
CDS Mutation	c.91G>A
AA Mutation	p.Glu31Lys(p.E31K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11105229:11105229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750126678
CDS Mutation	c.323C>T
AA Mutation	p.Thr108Met(p.T108M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11113678:11113678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755667663
CDS Mutation	c.1502C>T
AA Mutation	p.Ala501Val(p.A501V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11113380:11113380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289T>C
AA Mutation	p.Val430Ala(p.V430A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11116144:11116144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1637G>T
AA Mutation	p.Gly546Val(p.G546V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11131312:11131312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs13306505
CDS Mutation	c.2579C>T
AA Mutation	p.Ala860Val(p.A860V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11116204:11116204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1697T>C
AA Mutation	p.Ile566Thr(p.I566T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11106642:11106642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772G>A
AA Mutation	p.Glu258Lys(p.E258K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11116149:11116149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642A>G
AA Mutation	p.Asn548Asp(p.N548D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558518
Start	11102740:11102740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777640882
CDS Mutation	c.267C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558518
Start	11123250:11123250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2217G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558518
Start	11129601:11129601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774831273
CDS Mutation	c.2478C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558518
Start	11113559:11113559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764929176
CDS Mutation	c.1383C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558518
Start	11111578:11111578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558518
Start	11113312:11113312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1221C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000558518
Start	11106587:11106587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000558518
Start	11120189:11120189(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1946delC
AA Mutation	p.Pro649GlnfsTer16(p.P649Qfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LDLR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000558518
Start	11089569:11089569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21A>C
AA Mutation	p.Lys7Asn(p.K7N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript