Colon Cancer: Gene >> RASSF5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000579436
Start	206538237:206538237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.523G>C
AA Mutation	p.Gly175Arg(p.G175R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000579436
Start	206584543:206584543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.847C>A
AA Mutation	p.Pro283Thr(p.P283T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000579436
Start	206586927:206586927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1206T>G
AA Mutation	p.Phe402Leu(p.F402L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000579436
Start	206586928:206586928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1207A>T
AA Mutation	p.Arg403Trp(p.R403W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000579436
Start	206586969:206586969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1248A>C
AA Mutation	p.Lys416Asn(p.K416N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000579436
Start	206507912:206507912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Trp(p.R104W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000579436
Start	206507931:206507931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.329C>T
AA Mutation	p.Pro110Leu(p.P110L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000579436
Start	206584533:206584533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.837C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000579436
Start	206584452:206584452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781912138
CDS Mutation	c.756G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000579436
Start	206585211:206585211(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1024delC
AA Mutation	p.Leu342SerfsTer18(p.L342Sfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RASSF5

Mutation ID	1
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000579436
Start	206584655:206584655(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.963delT
AA Mutation	p.Phe321LeufsTer39(p.F321Lfs*39)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000579436
Start	206586955:206586955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1234G>T
AA Mutation	p.Glu412Ter(p.E412*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript