Colon Cancer: Gene >> SH3GL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269886
Start	4362732:4362732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150815092
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Trp(p.R245W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269886
Start	4365518:4365518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.295C>T
AA Mutation	p.Arg99Cys(p.R99C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269886
Start	4362338:4362338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150284370
CDS Mutation	c.901C>T
AA Mutation	p.Arg301Trp(p.R301W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269886
Start	4366967:4366967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Glu25Lys(p.E25K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269886
Start	4366527:4366527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.161C>T
AA Mutation	p.Thr54Ile(p.T54I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269886
Start	4365605:4365605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.208A>G
AA Mutation	p.Met70Val(p.M70V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269886
Start	4365531:4365531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758399287
CDS Mutation	c.282C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SH3GL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269886
Start	4362660:4362660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805G>C
AA Mutation	p.Glu269Gln(p.E269Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269886
Start	4361651:4361651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534214854
CDS Mutation	c.1056G>A
Mutation Classification	Silent
Feature Type	Transcript