Colon Cancer: Gene >> CAPN7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253693
Start	15242188:15242188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1799C>T
AA Mutation	p.Ala600Val(p.A600V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000253693
Start	15245669:15245669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2008C>T
AA Mutation	p.Arg670Trp(p.R670W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000253693
Start	15246793:15246793(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776786847
CDS Mutation	c.2072G>A
AA Mutation	p.Arg691Gln(p.R691Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000253693
Start	15246745:15246745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755588973
CDS Mutation	c.2024G>A
AA Mutation	p.Cys675Tyr(p.C675Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253693
Start	15218482:15218482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379A>C
AA Mutation	p.Thr127Pro(p.T127P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253693
Start	15227898:15227898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.785T>C
AA Mutation	p.Val262Ala(p.V262A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000253693
Start	15240849:15240849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1648C>A
AA Mutation	p.His550Asn(p.H550N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000253693
Start	15218493:15218493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390A>C
AA Mutation	p.Lys130Asn(p.K130N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000253693
Start	15240518:15240518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1453T>C
AA Mutation	p.Trp485Arg(p.W485R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253693
Start	15242189:15242189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531043006
CDS Mutation	c.1800G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253693
Start	15246779:15246779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772620309
CDS Mutation	c.2058C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253693
Start	15227870:15227870(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.759delA
AA Mutation	p.Lys253AsnfsTer21(p.K253Nfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CAPN7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253693
Start	15212189:15212189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188G>T
AA Mutation	p.Arg63Ile(p.R63I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253693
Start	15240803:15240803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602T>G
AA Mutation	p.Ile534Met(p.I534M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript