Colon Cancer: Gene >> NLRX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119173523:119173523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754221240
CDS Mutation	c.274C>T
AA Mutation	p.Arg92Trp(p.R92W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119181212:119181212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2309T>C
AA Mutation	p.Leu770Pro(p.L770P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119180165:119180165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2144T>C
AA Mutation	p.Val715Ala(p.V715A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119179962:119179962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1941G>T
AA Mutation	p.Lys647Asn(p.K647N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119174618:119174618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1015G>A
AA Mutation	p.Gly339Ser(p.G339S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119179816:119179816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1795G>A
AA Mutation	p.Ala599Thr(p.A599T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119174540:119174540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937T>A
AA Mutation	p.Ser313Thr(p.S313T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119180129:119180129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752216780
CDS Mutation	c.2108T>C
AA Mutation	p.Leu703Pro(p.L703P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119180214:119180214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2193C>G
AA Mutation	p.Asn731Lys(p.N731K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119172978:119172978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>T
AA Mutation	p.Ala73Val(p.A73V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119182228:119182228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2489A>G
AA Mutation	p.Gln830Arg(p.Q830R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119180141:119180141(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146800118
CDS Mutation	c.2120G>A
AA Mutation	p.Arg707His(p.R707H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119180056:119180056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2035C>A
AA Mutation	p.Leu679Ile(p.L679I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292199
Start	119175271:119175271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1668C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292199
Start	119173912:119173912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.663G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292199
Start	119182109:119182109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2370G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292199
Start	119172418:119172418(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.137delC
AA Mutation	p.Pro46LeufsTer12(p.P46Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292199
Start	119179902:119179902(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771726683
CDS Mutation	c.1887delG
AA Mutation	p.Leu630PhefsTer10(p.L630Ffs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292199
Start	119183169:119183169(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2663delG
AA Mutation	p.Gly888ValfsTer13(p.G888Vfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000292199
Start	119173672:119173672(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs767102699
CDS Mutation	c.428delC
AA Mutation	p.Pro143HisfsTer81(p.P143Hfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NLRX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119183429:119183429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2918C>A
AA Mutation	p.Ser973Tyr(p.S973Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119174043:119174043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199476042
CDS Mutation	c.794C>T
AA Mutation	p.Pro265Leu(p.P265L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000292199
Start	119174606:119174606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778713378
CDS Mutation	c.1003G>A
AA Mutation	p.Val335Ile(p.V335I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292199
Start	119175266:119175266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1663C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000292199
Start	119179830:119179830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142623204
CDS Mutation	c.1809C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000292199
Start	119179771:119179771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776884246
CDS Mutation	c.1750C>T
AA Mutation	p.Arg584Ter(p.R584*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript