Colon Cancer: Gene >> DSG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31333634:31333634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>T
AA Mutation	p.Gly244Cys(p.G244C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31340012:31340012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1674C>A
AA Mutation	p.Phe558Leu(p.F558L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31330028:31330028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509C>A
AA Mutation	p.Ser170Tyr(p.S170Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31327000:31327000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211G>A
AA Mutation	p.Ala71Thr(p.A71T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31328229:31328229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770916767
CDS Mutation	c.257G>A
AA Mutation	p.Arg86His(p.R86H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31336374:31336374(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1026G>A
AA Mutation	p.Met342Ile(p.M342I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31354961:31354961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2765T>C
AA Mutation	p.Val922Ala(p.V922A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31355173:31355173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2977G>A
AA Mutation	p.Gly993Arg(p.G993R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31354973:31354973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2777T>C
AA Mutation	p.Val926Ala(p.V926A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31329925:31329925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406G>T
AA Mutation	p.Asp136Tyr(p.D136Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31334163:31334163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.966G>A
AA Mutation	p.Met322Ile(p.M322I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31326880:31326880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91G>T
AA Mutation	p.Asp31Tyr(p.D31Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31346137:31346137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771756989
CDS Mutation	c.2039C>A
AA Mutation	p.Ser680Tyr(p.S680Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257192
Start	31354365:31354365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372254735
CDS Mutation	c.2169C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257192
Start	31354329:31354329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2133A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257192
Start	31354905:31354905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2709T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257192
Start	31355259:31355259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3063T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	protein_altering_variant
Transcription ID	ENST00000257192
Start	31343569:31343570(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1807_1808insTGGTGGTGG
AA Mutation	p.Gln603delinsLeuValValGlu(p.Q603delinsLVVE)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> DSG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31339969:31339969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1631T>C
AA Mutation	p.Val544Ala(p.V544A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31326880:31326880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.91G>T
AA Mutation	p.Asp31Tyr(p.D31Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000257192
Start	31334171:31334171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974G>T
AA Mutation	p.Arg325Ile(p.R325I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257192
Start	31333594:31333594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781133396
CDS Mutation	c.690C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257192
Start	31326951:31326951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778383508
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000257192
Start	31354605:31354605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747276192
CDS Mutation	c.2409C>T
Mutation Classification	Silent
Feature Type	Transcript