Colon Cancer: Gene >> LRPPRC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43899554:43899554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3621G>T
AA Mutation	p.Glu1207Asp(p.E1207D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43982426:43982426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.158T>C
AA Mutation	p.Leu53Pro(p.L53P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43979843:43979843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.452A>G
AA Mutation	p.Asp151Gly(p.D151G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43896680:43896680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373042003
CDS Mutation	c.3854C>T
AA Mutation	p.Pro1285Leu(p.P1285L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43977240:43977240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506T>G
AA Mutation	p.Leu169Arg(p.L169R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43894614:43894614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3916T>C
AA Mutation	p.Ser1306Pro(p.S1306P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43960604:43960604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1519T>G
AA Mutation	p.Phe507Val(p.F507V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260665
Start	43974151:43974151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182612310
CDS Mutation	c.1154C>T
AA Mutation	p.Thr385Met(p.T385M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43901344:43901344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3545A>G
AA Mutation	p.Asn1182Ser(p.N1182S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43973627:43973627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754172387
CDS Mutation	c.1349G>A
AA Mutation	p.Arg450Gln(p.R450Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260665
Start	43901385:43901385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113550898
CDS Mutation	c.3504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260665
Start	43934247:43934247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111847942
CDS Mutation	c.2679T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260665
Start	43905777:43905777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764087602
CDS Mutation	c.3279G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260665
Start	43974159:43974159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000260665
Start	43918026:43918026(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs776970160
CDS Mutation	c.3147delA
AA Mutation	p.Ala1051HisfsTer6(p.A1051Hfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LRPPRC

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260665
Start	43896706:43896706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3828A>T
AA Mutation	p.Arg1276Ser(p.R1276S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43947749:43947749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1947G>T
AA Mutation	p.Lys649Asn(p.K649N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43888607:43888607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4178C>A
AA Mutation	p.Ser1393Tyr(p.S1393Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260665
Start	43943853:43943853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2338C>T
AA Mutation	p.Leu780Phe(p.L780F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260665
Start	43905717:43905717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260665
Start	43925938:43925938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2760T>G
Mutation Classification	Silent
Feature Type	Transcript