Colon Cancer: Gene >> GBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89056101:89056101(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1283C>T
AA Mutation	p.Ser428Leu(p.S428L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89054814:89054814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1533A>C
AA Mutation	p.Arg511Ser(p.R511S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370473
Start	89056227:89056227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748915855
CDS Mutation	c.1157C>T
AA Mutation	p.Ala386Val(p.A386V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89058136:89058136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372549555
CDS Mutation	c.730C>T
AA Mutation	p.Arg244Cys(p.R244C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89056224:89056224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160A>G
AA Mutation	p.Gln387Arg(p.Q387R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89053406:89053406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1728A>G
AA Mutation	p.Ile576Met(p.I576M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89063080:89063080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.155C>A
AA Mutation	p.Ser52Tyr(p.S52Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89056087:89056087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1297T>C
AA Mutation	p.Tyr433His(p.Y433H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89063176:89063176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758858682
CDS Mutation	c.59G>A
AA Mutation	p.Arg20Gln(p.R20Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89063108:89063108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746630945
CDS Mutation	c.127A>G
AA Mutation	p.Ile43Val(p.I43V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370473
Start	89056962:89056962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1047C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370473
Start	89057999:89057999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757373270
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370473
Start	89059013:89059013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370473
Start	89058893:89058893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.579A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370473
Start	89053427:89053427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1707C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370473
Start	89056212:89056212(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1172delA
AA Mutation	p.Lys391SerfsTer28(p.K391Sfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370473
Start	89058221:89058221(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.645delA
AA Mutation	p.Asp216MetfsTer51(p.D216Mfs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370473
Start	89060262:89060262(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.253delC
AA Mutation	p.His85ThrfsTer9(p.H85Tfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370473
Start	89057066:89057066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943G>A
AA Mutation	p.Ala315Thr(p.A315T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370473
Start	89056100:89056100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761745237
CDS Mutation	c.1284G>A
Mutation Classification	Silent
Feature Type	Transcript