Colon Cancer: Gene >> OPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193654896:193654896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1882G>T
AA Mutation	p.Val628Leu(p.V628L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193664895:193664895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2512C>T
AA Mutation	p.His838Tyr(p.H838Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193614943:193614943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372435892
CDS Mutation	c.253C>T
AA Mutation	p.Arg85Cys(p.R85C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193648105:193648105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1741A>G
AA Mutation	p.Asn581Asp(p.N581D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193648828:193648828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1804C>T
AA Mutation	p.Leu602Phe(p.L602F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193662870:193662870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2404A>G
AA Mutation	p.Asn802Asp(p.N802D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193614915:193614915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225C>A
AA Mutation	p.Phe75Leu(p.F75L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193635424:193635424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.685T>G
AA Mutation	p.Tyr229Asp(p.Y229D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193614803:193614803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113G>A
AA Mutation	p.Arg38Gln(p.R38Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193617199:193617199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470C>T
AA Mutation	p.Pro157Leu(p.P157L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193666312:193666312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2630T>A
AA Mutation	p.Val877Glu(p.V877E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392438
Start	193648857:193648857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1833T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392438
Start	193614777:193614777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.87A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OPA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193644001:193644001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339A>G
AA Mutation	p.Ile447Val(p.I447V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193614803:193614803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.113G>A
AA Mutation	p.Arg38Gln(p.R38Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392438
Start	193657109:193657109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2043T>G
AA Mutation	p.Phe681Leu(p.F681L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript