Colon Cancer: Gene >> SELPLG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623882:108623882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.426G>T
AA Mutation	p.Gln142His(p.Q142H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623109:108623109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780303589
CDS Mutation	c.1199G>A
AA Mutation	p.Arg400His(p.R400H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623169:108623169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1139C>A
AA Mutation	p.Ala380Asp(p.A380D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108624042:108624042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201172154
CDS Mutation	c.266G>A
AA Mutation	p.Arg89His(p.R89H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623997:108623997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147444406
CDS Mutation	c.311C>T
AA Mutation	p.Thr104Met(p.T104M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623244:108623244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367836641
CDS Mutation	c.1064G>A
AA Mutation	p.Arg355His(p.R355H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623196:108623196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1112A>G
AA Mutation	p.Asp371Gly(p.D371G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000550948
Start	108623243:108623243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1065T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SELPLG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108623269:108623269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603289
CDS Mutation	c.1039C>T
AA Mutation	p.Arg347Cys(p.R347C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000550948
Start	108624175:108624175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372642040
CDS Mutation	c.133G>A
AA Mutation	p.Glu45Lys(p.E45K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript