Colon Cancer: Gene >> SPRR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295367
Start	153003306:153003306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286C>T
AA Mutation	p.Pro96Ser(p.P96S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000295367
Start	153003180:153003180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160C>T
AA Mutation	p.Pro54Ser(p.P54S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000295367
Start	153003119:153003119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.99T>A
AA Mutation	p.Phe33Leu(p.F33L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000295367
Start	153003110:153003110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746832933
CDS Mutation	c.90G>T
AA Mutation	p.Gln30His(p.Q30H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000295367
Start	153003189:153003189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.169G>T
AA Mutation	p.Gly57Cys(p.G57C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SPRR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295367
Start	153003067:153003067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.47T>C
AA Mutation	p.Leu16Pro(p.L16P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript