Colon Cancer: Gene >> NLRC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3564422:3564422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767898156
CDS Mutation	c.515C>T
AA Mutation	p.Ser172Leu(p.S172L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3548688:3548688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778330894
CDS Mutation	c.2669G>A
AA Mutation	p.Arg890His(p.R890H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3564222:3564222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.715C>T
AA Mutation	p.Pro239Ser(p.P239S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3542260:3542260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3038C>T
AA Mutation	p.Ser1013Phe(p.S1013F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3561717:3561717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148712383
CDS Mutation	c.2000G>A
AA Mutation	p.Arg667His(p.R667H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3557611:3557611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2081G>A
AA Mutation	p.Arg694Lys(p.R694K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3565000:3565000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373378033
CDS Mutation	c.37G>A
AA Mutation	p.Gly13Ser(p.G13S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3563778:3563778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753539558
CDS Mutation	c.1159G>A
AA Mutation	p.Glu387Lys(p.E387K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3564260:3564260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202116008
CDS Mutation	c.677C>T
AA Mutation	p.Thr226Met(p.T226M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3563144:3563144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1793C>T
AA Mutation	p.Pro598Leu(p.P598L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3549167:3549167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2578G>A
AA Mutation	p.Ala860Thr(p.A860T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3564176:3564176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761G>A
AA Mutation	p.Arg254His(p.R254H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359128
Start	3563212:3563212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1725G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359128
Start	3564340:3564340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359128
Start	3563170:3563170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1767C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359128
Start	3564703:3564703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747375398
CDS Mutation	c.234G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359128
Start	3548191:3548191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376394054
CDS Mutation	c.2715C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359128
Start	3563578:3563578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1359C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359128
Start	3561740:3561740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751567117
CDS Mutation	c.1977C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000359128
Start	3561789:3561789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1929-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NLRC3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3564434:3564434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.503G>A
AA Mutation	p.Gly168Asp(p.G168D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3563831:3563831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1106G>A
AA Mutation	p.Arg369Lys(p.R369K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3564279:3564279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762715807
CDS Mutation	c.658G>A
AA Mutation	p.Gly220Ser(p.G220S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359128
Start	3563369:3563369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756951899
CDS Mutation	c.1568C>T
AA Mutation	p.Pro523Leu(p.P523L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359128
Start	3564505:3564505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756551076
CDS Mutation	c.432C>T
Mutation Classification	Silent
Feature Type	Transcript