Colon Cancer: Gene >> N4BP2L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32443108:32443108(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1429A>G
AA Mutation	p.Asn477Asp(p.N477D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32536021:32536021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007A>C
AA Mutation	p.Glu336Ala(p.E336A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32442954:32442954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1583T>C
AA Mutation	p.Leu528Ser(p.L528S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32442676:32442676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1861G>A
AA Mutation	p.Glu621Lys(p.E621K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32521427:32521427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496T>C
AA Mutation	p.Val499Ala(p.V499A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32442774:32442774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1763C>T
AA Mutation	p.Ala588Val(p.A588V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32517980:32517980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs117678407
CDS Mutation	c.1574G>A
AA Mutation	p.Arg525Gln(p.R525Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32517948:32517948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1606G>A
AA Mutation	p.Glu536Lys(p.E536K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32443044:32443044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1493A>T
AA Mutation	p.Asn498Ile(p.N498I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32521406:32521406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1517C>G
AA Mutation	p.Thr506Ser(p.T506S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32443215:32443215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1322A>T
AA Mutation	p.Lys441Ile(p.K441I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32443787:32443787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758257794
CDS Mutation	c.750G>T
AA Mutation	p.Lys250Asn(p.K250N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32536828:32536828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.200A>C
AA Mutation	p.Tyr67Ser(p.Y67S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32517827:32517827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752218341
CDS Mutation	c.1727G>A
AA Mutation	p.Arg576His(p.R576H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32536388:32536388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>A
AA Mutation	p.Leu214Ile(p.L214I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32522220:32522220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1435A>G
AA Mutation	p.Asn479Asp(p.N479D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32522226:32522226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1429A>G
AA Mutation	p.Asn477Asp(p.N477D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267068
Start	32521405:32521405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1518T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399396
Start	32442761:32442761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1776A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399396
Start	32442410:32442410(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2127delT
AA Mutation	p.Phe709LeufsTer25(p.F709Lfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000267068
Start	32536865:32536865(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.163delG
AA Mutation	p.Val55SerfsTer3(p.V55Sfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399396
Start	32443851:32443851(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.686delA
AA Mutation	p.Asn229IlefsTer14(p.N229Ifs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000399396
Start	32442779:32442779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1758C>A
AA Mutation	p.Cys586Ter(p.C586*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained;inframe_insertion
Transcription ID	ENST00000399396
Start	32443258:32443259(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1278_1279insTAA
AA Mutation	p.Val426_Ala427insTer(p.V426_A427ins*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399396
Start	32443085:32443086(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1451dupA
AA Mutation	p.Asn484LysfsTer2(p.N484Kfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000399396
Start	32443259:32443260(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1277_1278insTGAG
AA Mutation	p.Ala427GlufsTer22(p.A427Efs*22)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> N4BP2L2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32536365:32536365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663G>T
AA Mutation	p.Lys221Asn(p.K221N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32443846:32443846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691G>T
AA Mutation	p.Asp231Tyr(p.D231Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32517942:32517942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1612C>A
AA Mutation	p.Gln538Lys(p.Q538K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32442676:32442676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1861G>A
AA Mutation	p.Glu621Lys(p.E621K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000399396
Start	32443787:32443787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758257794
CDS Mutation	c.750G>T
AA Mutation	p.Lys250Asn(p.K250N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000267068
Start	32536361:32536361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.667G>T
AA Mutation	p.Asp223Tyr(p.D223Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000267068
Start	32536695:32536695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749078055
CDS Mutation	c.333C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000399396
Start	32443892:32443892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766569836
CDS Mutation	c.645C>T
Mutation Classification	Silent
Feature Type	Transcript