Colon Cancer: Gene >> PHLDB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118627485:118627485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.662C>A
AA Mutation	p.Pro221Gln(p.P221Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118627845:118627845(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369034044
CDS Mutation	c.1022C>T
AA Mutation	p.Ala341Val(p.A341V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000361417
Start	118645736:118645736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137998974
CDS Mutation	c.3418G>A
AA Mutation	p.Ala1140Thr(p.A1140T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118627544:118627544(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191697288
CDS Mutation	c.721G>A
AA Mutation	p.Ala241Thr(p.A241T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118650186:118650186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3764G>A
AA Mutation	p.Ser1255Asn(p.S1255N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118627500:118627500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.677C>A
AA Mutation	p.Ala226Asp(p.A226D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118631929:118631929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2117G>A
AA Mutation	p.Ser706Asn(p.S706N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118643924:118643924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782158725
CDS Mutation	c.3002G>A
AA Mutation	p.Arg1001His(p.R1001H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118635400:118635400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2387A>G
AA Mutation	p.Glu796Gly(p.E796G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118627484:118627484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782775207
CDS Mutation	c.661C>T
AA Mutation	p.Pro221Ser(p.P221S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118639238:118639238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782014795
CDS Mutation	c.2723C>T
AA Mutation	p.Ser908Leu(p.S908L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118645524:118645524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201439807
CDS Mutation	c.3290C>T
AA Mutation	p.Ala1097Val(p.A1097V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118628220:118628220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140294013
CDS Mutation	c.1397G>A
AA Mutation	p.Arg466Gln(p.R466Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361417
Start	118642313:118642313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782508605
CDS Mutation	c.2796C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361417
Start	118645456:118645456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3222A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361417
Start	118642370:118642370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781792662
CDS Mutation	c.2853C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361417
Start	118628236:118628236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368906730
CDS Mutation	c.1413G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361417
Start	118645741:118645741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3423T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361417
Start	118628246:118628246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361417
Start	118645568:118645568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3334C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361417
Start	118628549:118628549(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1730delA
AA Mutation	p.Asn577IlefsTer42(p.N577Ifs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PHLDB1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361417
Start	118628069:118628069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>G
AA Mutation	p.Leu416Val(p.L416V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript