Colon Cancer: Gene >> SPOCK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317376
Start	72066983:72066983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760437901
CDS Mutation	c.847C>T
AA Mutation	p.Arg283Cys(p.R283C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317376
Start	72062777:72062777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369530712
CDS Mutation	c.1258G>A
AA Mutation	p.Gly420Arg(p.G420R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317376
Start	72067015:72067015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815C>T
AA Mutation	p.Ala272Val(p.A272V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317376
Start	72072168:72072168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.335T>C
AA Mutation	p.Ile112Thr(p.I112T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317376
Start	72064188:72064188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981G>T
AA Mutation	p.Lys327Asn(p.K327N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317376
Start	72068248:72068248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150144417
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000317376
Start	72064232:72064233(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.936dupC
AA Mutation	p.Cys313LeufsTer37(p.C313Lfs*37)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SPOCK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317376
Start	72072162:72072162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs577728856
CDS Mutation	c.341G>A
AA Mutation	p.Arg114His(p.R114H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript