Colon Cancer: Gene >> NLRP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	281463:281463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1729C>T
AA Mutation	p.Arg577Trp(p.R577W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	281136:281136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402C>A
AA Mutation	p.Leu468Met(p.L468M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	281335:281335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1601C>G
AA Mutation	p.Ala534Gly(p.A534G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	284391:284391(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2363A>T
AA Mutation	p.Gln788Leu(p.Q788L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	280822:280822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774708807
CDS Mutation	c.1088G>A
AA Mutation	p.Arg363Gln(p.R363Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	284291:284291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2263G>A
AA Mutation	p.Ala755Thr(p.A755T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	280802:280802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1068G>C
AA Mutation	p.Lys356Asn(p.K356N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	281405:281405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1671C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	280784:280784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765110010
CDS Mutation	c.1050C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	280763:280763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1029C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	280109:280109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	280823:280823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1089G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	281834:281834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2100C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312165
Start	281681:281681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1947G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000312165
Start	281782:281784(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs754832325
CDS Mutation	c.2050_2052delGAG
AA Mutation	p.Glu684del(p.E684del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000312165
Start	280794:280796(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs569773740
CDS Mutation	c.1066_1068delAAG
AA Mutation	p.Lys356del(p.K356del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NLRP6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312165
Start	281403:281403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1669C>T
AA Mutation	p.Arg557Cys(p.R557C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript