Colon Cancer: Gene >> DLG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77842029:77842029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289G>A
AA Mutation	p.Ser430Asn(p.S430N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77794930:77794930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5465C>T
AA Mutation	p.Pro1822Leu(p.P1822L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77842027:77842027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291G>A
AA Mutation	p.Glu431Lys(p.E431K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77829421:77829421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2119C>T
AA Mutation	p.Arg707Trp(p.R707W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77842003:77842003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1315C>T
AA Mutation	p.Arg439Cys(p.R439C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77829420:77829420(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2120G>A
AA Mutation	p.Arg707Gln(p.R707Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77828923:77828923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2248G>A
AA Mutation	p.Ala750Thr(p.A750T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77821464:77821464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748210887
CDS Mutation	c.3020C>T
AA Mutation	p.Ala1007Val(p.A1007V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77805730:77805730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5099C>A
AA Mutation	p.Ser1700Tyr(p.S1700Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77792490:77792490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140994758
CDS Mutation	c.5710G>A
AA Mutation	p.Val1904Ile(p.V1904I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77830815:77830815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1807A>C
AA Mutation	p.Ser603Arg(p.S603R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77812357:77812357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762391739
CDS Mutation	c.4046G>A
AA Mutation	p.Arg1349His(p.R1349H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77843637:77843637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>A
AA Mutation	p.Val312Met(p.V312M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77812334:77812334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4069T>C
AA Mutation	p.Ser1357Pro(p.S1357P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372391
Start	77821742:77821742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2742G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372391
Start	77822087:77822087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2397C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372391
Start	77821902:77821902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2582delC
AA Mutation	p.Pro861GlnfsTer32(p.P861Qfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372391
Start	77819921:77819921(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3500delC
AA Mutation	p.Pro1167ArgfsTer16(p.P1167Rfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000372391
Start	77835865:77835865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1495C>T
AA Mutation	p.Arg499Ter(p.R499*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000372391
Start	77816666:77816666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3910C>T
AA Mutation	p.Gln1304Ter(p.Q1304*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372391
Start	77805849:77805850(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.4979_4980insG
AA Mutation	p.Phe1661IlefsTer9(p.F1661Ifs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DLG5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77816572:77816572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4004T>C
AA Mutation	p.Leu1335Pro(p.L1335P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372391
Start	77812039:77812039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4207C>T
AA Mutation	p.Arg1403Trp(p.R1403W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000372391
Start	77853402:77853402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript