Colon Cancer: Gene >> LRRFIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237753465:237753465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760008859
CDS Mutation	c.640G>A
AA Mutation	p.Glu214Lys(p.E214K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237762612:237762612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.899G>C
AA Mutation	p.Ser300Thr(p.S300T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237763311:237763311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1598C>T
AA Mutation	p.Thr533Ile(p.T533I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237719535:237719535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778247171
CDS Mutation	c.166C>T
AA Mutation	p.Arg56Cys(p.R56C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237760158:237760158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842C>T
AA Mutation	p.Thr281Ile(p.T281I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237763179:237763179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771082673
CDS Mutation	c.1466C>T
AA Mutation	p.Ala489Val(p.A489V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237719536:237719536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371410588
CDS Mutation	c.167G>A
AA Mutation	p.Arg56His(p.R56H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237763507:237763507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1794G>T
AA Mutation	p.Gln598His(p.Q598H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237764027:237764027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566068988
CDS Mutation	c.2314G>A
AA Mutation	p.Asp772Asn(p.D772N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237760161:237760161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.845A>C
AA Mutation	p.Lys282Thr(p.K282T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392000
Start	237763180:237763180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776827427
CDS Mutation	c.1467G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392000
Start	237763729:237763729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2016T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392000
Start	237762676:237762676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.963T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392000
Start	237764026:237764026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137950221
CDS Mutation	c.2313C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000392000
Start	237763771:237763772(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2058_2059insACATTTTCAC
AA Mutation	p.Ser687ThrfsTer11(p.S687Tfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> LRRFIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237760115:237760115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780318201
CDS Mutation	c.799G>A
AA Mutation	p.Asp267Asn(p.D267N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000392000
Start	237720791:237720791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764869813
CDS Mutation	c.218G>A
AA Mutation	p.Arg73His(p.R73H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000392000
Start	237762637:237762637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758689322
CDS Mutation	c.924C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000392000
Start	237762659:237762659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.946G>T
AA Mutation	p.Glu316Ter(p.E316*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript