Colon Cancer: Gene >> RASSF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361228
Start	85805873:85805873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.137G>A
AA Mutation	p.Arg46His(p.R46H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361228
Start	85804958:85804958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1052A>G
AA Mutation	p.Gln351Arg(p.Q351R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361228
Start	85805123:85805123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887T>A
AA Mutation	p.Ile296Asn(p.I296N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361228
Start	85805461:85805461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.549G>A
AA Mutation	p.Met183Ile(p.M183I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361228
Start	85805356:85805356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361228
Start	85805125:85805125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361228
Start	85805212:85805212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.798T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361228
Start	85805593:85805593(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.417delA
AA Mutation	p.Lys139AsnfsTer11(p.K139Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000361228
Start	85804944:85804944(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066G>T
AA Mutation	p.Glu356Ter(p.E356*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361228
Start	85805698:85805699(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.311dupG
AA Mutation	p.Asp105ArgfsTer2(p.D105Rfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361228
Start	85805082:85805083(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.927_928insTCTCTTT
AA Mutation	p.Leu310SerfsTer7(p.L310Sfs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000361228
Start	85805084:85805085(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.925_926insTATTT
AA Mutation	p.Glu309ValfsTer9(p.E309Vfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RASSF9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361228
Start	85805180:85805180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369886202
CDS Mutation	c.830G>A
AA Mutation	p.Arg277Gln(p.R277Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361228
Start	85805890:85805890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000361228
Start	85805196:85805196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Ter(p.R272*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript