Colon Cancer: Gene >> CBFA2T2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33624889:33624889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845G>A
AA Mutation	p.Gly282Asp(p.G282D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33629780:33629780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145709031
CDS Mutation	c.1121G>A
AA Mutation	p.Arg374His(p.R374H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33619563:33619563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494C>A
AA Mutation	p.Ala165Asp(p.A165D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33611301:33611301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413G>A
AA Mutation	p.Gly138Glu(p.G138E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33629797:33629797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138C>T
AA Mutation	p.Arg380Cys(p.R380C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33644554:33644554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758482628
CDS Mutation	c.1723G>A
AA Mutation	p.Val575Met(p.V575M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33644518:33644518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1687G>A
AA Mutation	p.Gly563Ser(p.G563S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33628427:33628427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1051C>A
AA Mutation	p.Leu351Ile(p.L351I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33640371:33640371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1355C>T
AA Mutation	p.Ala452Val(p.A452V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000346541
Start	33611313:33611313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs549957667
CDS Mutation	c.425G>A
AA Mutation	p.Arg142Gln(p.R142Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346541
Start	33624875:33624875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.831C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000346541
Start	33623282:33623282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.705G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000346541
Start	33636698:33636698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1314G>A
AA Mutation	p.Trp438Ter(p.W438*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CBFA2T2

No Mutation Annotation!