Colon Cancer: Gene >> XIRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39187620:39187620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1826A>C
AA Mutation	p.Lys609Thr(p.K609T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39188125:39188125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321T>C
AA Mutation	p.Phe441Leu(p.F441L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39186288:39186288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3158C>T
AA Mutation	p.Ala1053Val(p.A1053V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39184185:39184185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548931854
CDS Mutation	c.5261C>T
AA Mutation	p.Thr1754Met(p.T1754M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39187825:39187825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621G>A
AA Mutation	p.Glu541Lys(p.E541K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39189396:39189396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50C>T
AA Mutation	p.Ala17Val(p.A17V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39186613:39186613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs187061436
CDS Mutation	c.2833C>T
AA Mutation	p.Arg945Trp(p.R945W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39186778:39186778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754187803
CDS Mutation	c.2668G>A
AA Mutation	p.Val890Met(p.V890M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39187414:39187414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116921702
CDS Mutation	c.2032C>T
AA Mutation	p.Arg678Trp(p.R678W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39186819:39186819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2627C>T
AA Mutation	p.Pro876Leu(p.P876L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39187413:39187413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143151548
CDS Mutation	c.2033G>A
AA Mutation	p.Arg678Gln(p.R678Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39186161:39186161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3285A>C
AA Mutation	p.Lys1095Asn(p.K1095N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39188523:39188523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751411277
CDS Mutation	c.923G>A
AA Mutation	p.Arg308His(p.R308H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39184474:39184474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749205423
CDS Mutation	c.4972C>T
AA Mutation	p.Arg1658Trp(p.R1658W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39185817:39185817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3629C>A
AA Mutation	p.Ala1210Glu(p.A1210E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39187298:39187298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752561906
CDS Mutation	c.2148C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39187850:39187850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147610598
CDS Mutation	c.1596C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39187679:39187679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200190507
CDS Mutation	c.1767C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39188654:39188654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775040797
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39186392:39186392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3054A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39188318:39188318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1128T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39186599:39186599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751741273
CDS Mutation	c.2847G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39185006:39185006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4440C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39188849:39188849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39188417:39188417(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340369
Start	39188123:39188123(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1323delT
AA Mutation	p.Phe441LeufsTer39(p.F441Lfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340369
Start	39186044:39186044(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3402delG
AA Mutation	p.Trp1135GlyfsTer2(p.W1135Gfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340369
Start	39185853:39185853(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3593delG
AA Mutation	p.Gly1198AlafsTer29(p.G1198Afs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	stop_gained
Transcription ID	ENST00000340369
Start	39185053:39185053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4393C>T
AA Mutation	p.Gln1465Ter(p.Q1465*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000340369
Start	39187738:39187738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146353398
CDS Mutation	c.1708C>T
AA Mutation	p.Arg570Ter(p.R570*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000340369
Start	39186808:39186808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2638C>T
AA Mutation	p.Gln880Ter(p.Q880*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000340369
Start	39184280:39184282(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5164_5166delAAG
AA Mutation	p.Lys1722del(p.K1722del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> XIRP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39184557:39184557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4889A>G
AA Mutation	p.His1630Arg(p.H1630R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39187842:39187842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370513707
CDS Mutation	c.1604G>A
AA Mutation	p.Arg535Gln(p.R535Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340369
Start	39189162:39189162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371716831
CDS Mutation	c.284G>A
AA Mutation	p.Arg95His(p.R95H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39188609:39188609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340369
Start	39185705:39185705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770016283
CDS Mutation	c.3741G>A
Mutation Classification	Silent
Feature Type	Transcript