Colon Cancer: Gene >> SGCE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265735
Start	94598871:94598871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370800943
CDS Mutation	c.1157C>T
AA Mutation	p.Thr386Met(p.T386M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265735
Start	94629803:94629803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.148G>A
AA Mutation	p.Val50Ile(p.V50I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265735
Start	94628302:94628302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs11548285
CDS Mutation	c.290G>A
AA Mutation	p.Arg97Gln(p.R97Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265735
Start	94656067:94656067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32A>G
AA Mutation	p.Asp11Gly(p.D11G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265735
Start	94598802:94598802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545029310
CDS Mutation	c.1226C>T
AA Mutation	p.Thr409Ile(p.T409I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265735
Start	94656078:94656078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21G>T
AA Mutation	p.Trp7Cys(p.W7C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265735
Start	94598852:94598852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1176T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265735
Start	94656074:94656074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265735
Start	94600798:94600798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000265735
Start	94598882:94598882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146G>A
AA Mutation	p.Trp382Ter(p.W382*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000265735
Start	94603403:94603403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712G>T
AA Mutation	p.Glu238Ter(p.E238*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000265735
Start	94628303:94628303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs121908489
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Ter(p.R97*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SGCE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265735
Start	94600781:94600781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.902A>G
AA Mutation	p.Tyr301Cys(p.Y301C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265735
Start	94623379:94623379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557861177
CDS Mutation	c.409C>T
AA Mutation	p.Arg137Cys(p.R137C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265735
Start	94618823:94618823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597A>C
Mutation Classification	Silent
Feature Type	Transcript