Colon Cancer: Gene >> CAPN10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391984
Start	240591007:240591007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.466G>T
AA Mutation	p.Ala156Ser(p.A156S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391984
Start	240594031:240594031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814G>T
AA Mutation	p.Gly272Trp(p.G272W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000391984
Start	240596741:240596741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1542G>T
AA Mutation	p.Trp514Cys(p.W514C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000391984
Start	240594572:240594572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149240512
CDS Mutation	c.860C>T
AA Mutation	p.Ala287Val(p.A287V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000391984
Start	240590992:240590992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451C>A
AA Mutation	p.Leu151Met(p.L151M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000391984
Start	240593953:240593953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372639976
CDS Mutation	c.736C>T
AA Mutation	p.Arg246Trp(p.R246W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000391984
Start	240592033:240592033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571G>T
AA Mutation	p.Ala191Ser(p.A191S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000391984
Start	240595053:240595053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027C>T
AA Mutation	p.Pro343Ser(p.P343S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000391984
Start	240594568:240594568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.856G>A
AA Mutation	p.Ala286Thr(p.A286T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391984
Start	240596375:240596375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200314283
CDS Mutation	c.1335C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391984
Start	240596393:240596393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747760729
CDS Mutation	c.1353C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391984
Start	240590844:240590844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.303C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391984
Start	240596785:240596786(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs779173614
CDS Mutation	c.1592dupG
AA Mutation	p.Ser532GlnfsTer38(p.S532Qfs*38)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CAPN10

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391984
Start	240589438:240589438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758590960
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript