Colon Cancer: Gene >> DSG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31461273:31461273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370472156
CDS Mutation	c.860G>A
AA Mutation	p.Arg287Gln(p.R287Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31465401:31465401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770073709
CDS Mutation	c.1355G>A
AA Mutation	p.Arg452Gln(p.R452Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31460858:31460858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710T>C
AA Mutation	p.Val237Ala(p.V237A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31466610:31466610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145720587
CDS Mutation	c.1492G>A
AA Mutation	p.Glu498Lys(p.E498K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31459905:31459905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.578A>T
AA Mutation	p.Lys193Ile(p.K193I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31476022:31476022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2762C>A
AA Mutation	p.Ser921Tyr(p.S921Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31466730:31466730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144565301
CDS Mutation	c.1612G>A
AA Mutation	p.Val538Ile(p.V538I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31464173:31464173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1062A>T
AA Mutation	p.Glu354Asp(p.E354D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31466697:31466697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1579G>A
AA Mutation	p.Ala527Thr(p.A527T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31457072:31457072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164C>T
AA Mutation	p.Ala55Val(p.A55V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31458509:31458509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.281A>G
AA Mutation	p.Gln94Arg(p.Q94R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31460923:31460923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>T
AA Mutation	p.Asp259Tyr(p.D259Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31475653:31475653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2393T>G
AA Mutation	p.Phe798Cys(p.F798C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31464196:31464196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs73414212
CDS Mutation	c.1085G>A
AA Mutation	p.Arg362Gln(p.R362Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31475944:31475944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2684T>G
AA Mutation	p.Phe895Cys(p.F895C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31476249:31476249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2989C>T
AA Mutation	p.Arg997Cys(p.R997C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257189
Start	31465411:31465411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1365T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257189
Start	31475678:31475678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2418C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257189
Start	31472408:31472408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2022C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257189
Start	31476008:31476008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2748C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257189
Start	31464214:31464214(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1106delC
AA Mutation	p.Pro369GlnfsTer6(p.P369Qfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000257189
Start	31465363:31465363(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1321delA
AA Mutation	p.Thr441LeufsTer10(p.T441Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000257189
Start	31464246:31464246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1135G>T
AA Mutation	p.Glu379Ter(p.E379*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000257189
Start	31461272:31461272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.859C>T
AA Mutation	p.Arg287Ter(p.R287*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DSG3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31464310:31464310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199A>C
AA Mutation	p.Lys400Thr(p.K400T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31466577:31466577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771845317
CDS Mutation	c.1459G>A
AA Mutation	p.Asp487Asn(p.D487N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257189
Start	31465403:31465403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357G>T
AA Mutation	p.Asp453Tyr(p.D453Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript