Colon Cancer: Gene >> DSG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31536303:31536303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753406968
CDS Mutation	c.1525G>A
AA Mutation	p.Asp509Asn(p.D509N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31521168:31521168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.448C>A
AA Mutation	p.Leu150Ile(p.L150I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31545976:31545976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2590A>G
AA Mutation	p.Asn864Asp(p.N864D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31546367:31546367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2981C>A
AA Mutation	p.Pro994His(p.P994H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31542730:31542730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs397516705
CDS Mutation	c.2212G>A
AA Mutation	p.Ala738Thr(p.A738T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31541225:31541225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201564919
CDS Mutation	c.1912G>A
AA Mutation	p.Gly638Arg(p.G638R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31541256:31541256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1943C>A
AA Mutation	p.Pro648His(p.P648H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31522143:31522143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.584A>C
AA Mutation	p.Lys195Thr(p.K195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31535393:31535393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1404G>T
AA Mutation	p.Lys468Asn(p.K468N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31535382:31535382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1393T>C
AA Mutation	p.Tyr465His(p.Y465H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31535279:31535279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1290A>C
AA Mutation	p.Lys430Asn(p.K430N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31546099:31546099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2713G>A
AA Mutation	p.Glu905Lys(p.E905K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31524786:31524786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.912T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31536392:31536392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1614T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31546257:31546257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2871G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31522141:31522141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748768578
CDS Mutation	c.582G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31546092:31546092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2706A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261590
Start	31531061:31531061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372598337
CDS Mutation	c.1089G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261590
Start	31545914:31545914(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2533delA
AA Mutation	p.Ile845Ter(p.I845*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> DSG2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31545838:31545838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2452G>A
AA Mutation	p.Glu818Lys(p.E818K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261590
Start	31536385:31536385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1607A>C
AA Mutation	p.Lys536Thr(p.K536T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript