Colon Cancer: Gene >> KDM1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356634
Start	23083289:23083289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2484G>T
AA Mutation	p.Gln828His(p.Q828H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356634
Start	23019847:23019847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.251A>G
AA Mutation	p.Gln84Arg(p.Q84R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356634
Start	23072185:23072185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774064976
CDS Mutation	c.1538C>T
AA Mutation	p.Ala513Val(p.A513V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356634
Start	23082279:23082279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2286C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356634
Start	23068610:23068610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1179T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356634
Start	23050397:23050397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561679633
CDS Mutation	c.528C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356634
Start	23082348:23082348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759361794
CDS Mutation	c.2355G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000356634
Start	23077339:23077339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1774C>T
AA Mutation	p.Gln592Ter(p.Q592*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> KDM1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356634
Start	23055992:23055992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.884G>A
AA Mutation	p.Arg295Gln(p.R295Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356634
Start	23069128:23069128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1318G>A
AA Mutation	p.Glu440Lys(p.E440K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356634
Start	23081508:23081508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759735931
CDS Mutation	c.2161G>A
AA Mutation	p.Asp721Asn(p.D721N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356634
Start	23059088:23059088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1028C>A
AA Mutation	p.Ala343Asp(p.A343D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356634
Start	23030632:23030632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.515C>T
AA Mutation	p.Ser172Leu(p.S172L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356634
Start	23068631:23068631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1200C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356634
Start	23055130:23055130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189014649
CDS Mutation	c.792C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356634
Start	23079048:23079048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549024936
CDS Mutation	c.1854C>T
Mutation Classification	Silent
Feature Type	Transcript