Colon Cancer: Gene >> RNF111

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000557998
Start	59031081:59031081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259A>C
AA Mutation	p.Lys87Gln(p.K87Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000557998
Start	59094787:59094787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2872C>A
AA Mutation	p.Leu958Ile(p.L958I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000557998
Start	59091098:59091098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2683C>T
AA Mutation	p.Arg895Cys(p.R895C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000557998
Start	59084137:59084137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2306A>G
AA Mutation	p.His769Arg(p.H769R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000557998
Start	59058527:59058527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1343G>A
AA Mutation	p.Ser448Asn(p.S448N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000557998
Start	59076060:59076060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762937096
CDS Mutation	c.1793G>A
AA Mutation	p.Arg598Gln(p.R598Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000557998
Start	59066942:59066942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs75252387
CDS Mutation	c.1545T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000557998
Start	59076148:59076148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759371658
CDS Mutation	c.1881G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000557998
Start	59031068:59031068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.246G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000557998
Start	59066945:59066945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200399712
CDS Mutation	c.1548C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000557998
Start	59084144:59084144(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2318delC
AA Mutation	p.Pro773HisfsTer44(p.P773Hfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000557998
Start	59081212:59081213(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2227_2228delCA
AA Mutation	p.Gln743GlufsTer6(p.Q743Efs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000557998
Start	59031505:59031506(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.686_687delAA
AA Mutation	p.Lys229ArgfsTer23(p.K229Rfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000557998
Start	59080997:59080997(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2015delC
AA Mutation	p.Pro672LeufsTer42(p.P672Lfs*42)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000557998
Start	59085747:59085747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766065838
CDS Mutation	c.2512C>T
AA Mutation	p.Arg838Ter(p.R838*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000557998
Start	59076059:59076059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1792C>T
AA Mutation	p.Arg598Ter(p.R598*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RNF111

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000557998
Start	59052412:59052412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.988A>C
AA Mutation	p.Thr330Pro(p.T330P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000557998
Start	59031179:59031179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.357G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000557998
Start	59031520:59031520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.698T>G
AA Mutation	p.Leu233Ter(p.L233*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000557998
Start	59055839:59055839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165G>T
AA Mutation	p.Glu389Ter(p.E389*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript