Colon Cancer: Gene >> DLG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83980613:83980613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634G>T
AA Mutation	p.Gly212Trp(p.G212W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000398309
Start	83466816:83466816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2306G>A
AA Mutation	p.Gly769Asp(p.G769D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84059477:84059477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.442G>T
AA Mutation	p.Asp148Tyr(p.D148Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376104
Start	85111689:85111689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329C>A
AA Mutation	p.Pro110His(p.P110H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84059348:84059348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201416435
CDS Mutation	c.571G>A
AA Mutation	p.Val191Ile(p.V191I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84163508:84163508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771812946
CDS Mutation	c.262A>G
AA Mutation	p.Asn88Asp(p.N88D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83633215:83633215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1621G>A
AA Mutation	p.Val541Ile(p.V541I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84251287:84251287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.209G>C
AA Mutation	p.Ser70Thr(p.S70T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83472770:83472770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1986A>C
AA Mutation	p.Gln662His(p.Q662H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83786754:83786754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1446G>T
AA Mutation	p.Gln482His(p.Q482H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84059386:84059386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756739930
CDS Mutation	c.533G>A
AA Mutation	p.Arg178Gln(p.R178Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83930400:83930400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577146407
CDS Mutation	c.1109A>G
AA Mutation	p.Asp370Gly(p.D370G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84534582:84534582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192T>G
AA Mutation	p.Ile64Met(p.I64M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83962915:83962915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.995A>C
AA Mutation	p.Lys332Thr(p.K332T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83874462:83874462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199599488
CDS Mutation	c.1208G>A
AA Mutation	p.Arg403His(p.R403H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83484154:83484154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1953T>A
AA Mutation	p.Ser651Arg(p.S651R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83532736:83532736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1850C>T
AA Mutation	p.Ala617Val(p.A617V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84098944:84098944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413C>T
AA Mutation	p.Ala138Val(p.A138V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83541711:83541711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1773G>T
AA Mutation	p.Glu591Asp(p.E591D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83833661:83833661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1360C>T
AA Mutation	p.Pro454Ser(p.P454S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83633241:83633241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1595G>A
AA Mutation	p.Arg532Gln(p.R532Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83980598:83980598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649C>A
AA Mutation	p.Pro217Thr(p.P217T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84251254:84251254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781080266
CDS Mutation	c.242T>C
AA Mutation	p.Leu81Ser(p.L81S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000376104
Start	85285307:85285307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781361075
CDS Mutation	c.99G>T
AA Mutation	p.Lys33Asn(p.K33N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83833670:83833670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351G>A
AA Mutation	p.Ala451Thr(p.A451T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83466808:83466808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2314T>C
AA Mutation	p.Cys772Arg(p.C772R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84099040:84099040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.317C>T
AA Mutation	p.Ser106Phe(p.S106F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83471716:83471716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2041C>T
AA Mutation	p.Arg681Trp(p.R681W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83833763:83833763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1258C>T
AA Mutation	p.Arg420Cys(p.R420C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83980579:83980579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668A>T
AA Mutation	p.Tyr223Phe(p.Y223F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84251263:84251263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.233C>T
AA Mutation	p.Thr78Ile(p.T78I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83462020:83462020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2488T>A
AA Mutation	p.Phe830Ile(p.F830I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376104
Start	85111685:85111685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.333T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398309
Start	83633321:83633321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761605010
CDS Mutation	c.1515C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398309
Start	84163494:84163494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376104
Start	85285295:85285295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000398309
Start	83965382:83965382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.828T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000398309
Start	83541701:83541701(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1783delG
AA Mutation	p.Val595SerfsTer16(p.V595Sfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	stop_gained
Transcription ID	ENST00000398309
Start	84163478:84163478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292G>T
AA Mutation	p.Glu98Ter(p.E98*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	stop_gained
Transcription ID	ENST00000376104
Start	85285357:85285357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49G>T
AA Mutation	p.Glu17Ter(p.E17*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	stop_gained
Transcription ID	ENST00000398309
Start	84059366:84059366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.553C>T
AA Mutation	p.Arg185Ter(p.R185*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000398309
Start	84098922:84098922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.434+1G>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000398309
Start	83484128:83484128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1978+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> DLG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84534582:84534582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.192T>G
AA Mutation	p.Ile64Met(p.I64M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	84534701:84534701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.73C>T
AA Mutation	p.His25Tyr(p.H25Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000398309
Start	83930443:83930443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066G>A
AA Mutation	p.Asp356Asn(p.D356N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376104
Start	85285259:85285259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.147T>C
Mutation Classification	Silent
Feature Type	Transcript