Colon Cancer: Gene >> RAF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251849
Start	12604200:12604200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80338796
CDS Mutation	c.770C>T
AA Mutation	p.Ser257Leu(p.S257L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000251849
Start	12585797:12585797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1420A>T
AA Mutation	p.Ile474Leu(p.I474L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251849
Start	12591735:12591735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166C>T
AA Mutation	p.Ala389Val(p.A389V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000251849
Start	12618604:12618604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772390935
CDS Mutation	c.118C>T
AA Mutation	p.Arg40Cys(p.R40C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000251849
Start	12600155:12600155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987A>C
AA Mutation	p.Lys329Asn(p.K329N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000251849
Start	12585734:12585734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1483C>T
AA Mutation	p.Arg495Cys(p.R495C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000251849
Start	12608791:12608791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.556G>A
AA Mutation	p.Asp186Asn(p.D186N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251849
Start	12609248:12609248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RAF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251849
Start	12599702:12599702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097G>T
AA Mutation	p.Gly366Val(p.G366V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251849
Start	12585181:12585181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751232720
CDS Mutation	c.1609G>A
AA Mutation	p.Val537Ile(p.V537I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251849
Start	12608856:12608856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.491G>A
AA Mutation	p.Arg164Gln(p.R164Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251849
Start	12590896:12590896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142942142
CDS Mutation	c.1272C>T
Mutation Classification	Silent
Feature Type	Transcript