Colon Cancer: Gene >> RAB11FIP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31521926:31521926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.770C>T
AA Mutation	p.Thr257Met(p.T257M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31523591:31523591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1009G>A
AA Mutation	p.Asp337Asn(p.D337N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31523976:31523976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1113G>T
AA Mutation	p.Glu371Asp(p.E371D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31523960:31523960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1097G>A
AA Mutation	p.Ser366Asn(p.S366N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31521272:31521272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670G>A
AA Mutation	p.Asp224Asn(p.D224N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000621161
Start	31523609:31523609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027A>G
AA Mutation	p.Lys343Glu(p.K343E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31517802:31517802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488A>G
AA Mutation	p.Gln163Arg(p.Q163R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31523945:31523945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199789204
CDS Mutation	c.1082A>G
AA Mutation	p.Asn361Ser(p.N361S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31531688:31531688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144926498
CDS Mutation	c.1870G>A
AA Mutation	p.Ala624Thr(p.A624T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621161
Start	31521301:31521301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621161
Start	31523557:31523557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621161
Start	31434045:31434045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621161
Start	31521927:31521927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372143570
CDS Mutation	c.771G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621161
Start	31434113:31434113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570241764
CDS Mutation	c.327C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000621161
Start	31431879:31431880(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs751772020
CDS Mutation	c.232dupG
AA Mutation	p.Val78GlyfsTer46(p.V78Gfs*46)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RAB11FIP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31431820:31431820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167A>C
AA Mutation	p.Lys56Thr(p.K56T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31531688:31531688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144926498
CDS Mutation	c.1870G>A
AA Mutation	p.Ala624Thr(p.A624T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000621161
Start	31521348:31521348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.746C>T
AA Mutation	p.Ser249Leu(p.S249L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621161
Start	31530460:31530460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747610392
CDS Mutation	c.1788G>A
Mutation Classification	Silent
Feature Type	Transcript