Colon Cancer: Gene >> RASSF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4790590:4790590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398T>C
AA Mutation	p.Leu133Pro(p.L133P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4786249:4786249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.893T>C
AA Mutation	p.Val298Ala(p.V298A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4795879:4795879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.223G>A
AA Mutation	p.Glu75Lys(p.E75K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4795875:4795875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.227G>A
AA Mutation	p.Arg76His(p.R76H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4786234:4786234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192780679
CDS Mutation	c.908G>A
AA Mutation	p.Arg303His(p.R303H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4790563:4790563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747554035
CDS Mutation	c.425G>A
AA Mutation	p.Arg142His(p.R142H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4795914:4795914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748168721
CDS Mutation	c.188G>A
AA Mutation	p.Arg63His(p.R63H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379376
Start	4786308:4786308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200418178
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000379376
Start	4795863:4795863(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.239delC
AA Mutation	p.Pro80LeufsTer20(p.P80Lfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000379376
Start	4790501:4790501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487C>T
AA Mutation	p.Arg163Ter(p.R163*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000379376
Start	4784317:4784317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937C>T
AA Mutation	p.Arg313Ter(p.R313*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	start_lost
Transcription ID	ENST00000379376
Start	4801030:4801030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> RASSF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4795876:4795876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755440456
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Cys(p.R76C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4784338:4784338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.916A>G
AA Mutation	p.Thr306Ala(p.T306A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379376
Start	4795879:4795879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.223G>A
AA Mutation	p.Glu75Lys(p.E75K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379376
Start	4786308:4786308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200418178
CDS Mutation	c.834C>T
Mutation Classification	Silent
Feature Type	Transcript