Colon Cancer: Gene >> ING1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375774
Start	110719597:110719597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934G>A
AA Mutation	p.Asp312Asn(p.D312N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375774
Start	110715727:110715727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.284C>A
AA Mutation	p.Ala95Glu(p.A95E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375774
Start	110719501:110719501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838G>A
AA Mutation	p.Glu280Lys(p.E280K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375774
Start	110719795:110719795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1132T>C
AA Mutation	p.Trp378Arg(p.W378R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375774
Start	110715608:110715608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.165C>G
AA Mutation	p.Asn55Lys(p.N55K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375774
Start	110719673:110719673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376816952
CDS Mutation	c.1010C>T
AA Mutation	p.Ala337Val(p.A337V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000375774
Start	110719771:110719771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108G>T
AA Mutation	p.Asp370Tyr(p.D370Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000375774
Start	110719576:110719576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.913G>A
AA Mutation	p.Ala305Thr(p.A305T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375774
Start	110719365:110719365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375774
Start	110719749:110719749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1086C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375774
Start	110719464:110719464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000375774
Start	110719855:110719855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1192A>T
AA Mutation	p.Lys398Ter(p.K398*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000375774
Start	110719678:110719678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Ter(p.R339*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ING1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375774
Start	110719294:110719294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.631C>T
AA Mutation	p.Arg211Trp(p.R211W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000375774
Start	110719678:110719678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015C>T
AA Mutation	p.Arg339Ter(p.R339*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript