Colon Cancer: Gene >> SPIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375859
Start	88468537:88468537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.521C>A
AA Mutation	p.Pro174His(p.P174H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375859
Start	88468516:88468516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.500A>G
AA Mutation	p.Tyr167Cys(p.Y167C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375859
Start	88426574:88426574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751098696
CDS Mutation	c.35G>A
AA Mutation	p.Arg12Gln(p.R12Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375859
Start	88448969:88448969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.81G>T
AA Mutation	p.Met27Ile(p.M27I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375859
Start	88475259:88475259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771T>G
AA Mutation	p.Asp257Glu(p.D257E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375859
Start	88468448:88468448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432G>T
AA Mutation	p.Glu144Asp(p.E144D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000375859
Start	88462640:88462641(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.246_247insTTCAC
AA Mutation	p.Asn83PhefsTer9(p.N83Ffs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SPIN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375859
Start	88468381:88468381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365G>A
AA Mutation	p.Arg122Gln(p.R122Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript