Colon Cancer: Gene >> MAPRE2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300249
Start	35097583:35097583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756121791
CDS Mutation	c.388G>A
AA Mutation	p.Val130Ile(p.V130I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300249
Start	35101977:35101977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.428G>A
AA Mutation	p.Arg143His(p.R143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300249
Start	35097571:35097571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.376A>G
AA Mutation	p.Lys126Glu(p.K126E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300249
Start	35102048:35102048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499T>C
AA Mutation	p.Tyr167His(p.Y167H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300249
Start	35140305:35140305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920C>T
AA Mutation	p.Thr307Ile(p.T307I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300249
Start	35097459:35097459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300249
Start	35102124:35102125(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.581dupA
AA Mutation	p.Ser195ValfsTer13(p.S195Vfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAPRE2

No Mutation Annotation!