Colon Cancer: Gene >> LNX1

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263925
Start	53481854:53481854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351G>A
AA Mutation	p.Ala451Thr(p.A451T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53507403:53507403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689T>C
AA Mutation	p.Val230Ala(p.V230A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000263925
Start	53476753:53476753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143573829
CDS Mutation	c.1892G>A
AA Mutation	p.Arg631Gln(p.R631Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53478705:53478705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1523T>C
AA Mutation	p.Val508Ala(p.V508A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53508220:53508220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.388G>A
AA Mutation	p.Gly130Ser(p.G130S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53496216:53496216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1157A>C
AA Mutation	p.Lys386Thr(p.K386T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53478652:53478652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1576G>A
AA Mutation	p.Ala526Thr(p.A526T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53573654:53573654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Cys(p.R117C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53476850:53476850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1795G>A
AA Mutation	p.Glu599Lys(p.E599K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53496369:53496369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004T>C
AA Mutation	p.Val335Ala(p.V335A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53476934:53476934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1711C>T
AA Mutation	p.Arg571Trp(p.R571W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53460978:53460978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2116G>T
AA Mutation	p.Ala706Ser(p.A706S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263925
Start	53507444:53507444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263925
Start	53498746:53498746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000263925
Start	53478665:53478665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758332865
CDS Mutation	c.1563C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263925
Start	53507422:53507422(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.670delA
AA Mutation	p.Ile224Ter(p.I224*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263925
Start	53460911:53460911(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2183delT
AA Mutation	p.Leu728TyrfsTer20(p.L728Yfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LNX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53496369:53496369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1004T>C
AA Mutation	p.Val335Ala(p.V335A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53498696:53498696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs542109970
CDS Mutation	c.923G>A
AA Mutation	p.Arg308His(p.R308H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53498778:53498778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841G>T
AA Mutation	p.Asp281Tyr(p.D281Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263925
Start	53507994:53507994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201126543
CDS Mutation	c.614G>A
AA Mutation	p.Arg205Gln(p.R205Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000263925
Start	53478640:53478640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1588G>T
AA Mutation	p.Glu530Ter(p.E530*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript