Colon Cancer: Gene >> NUAK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067173:106067173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1615G>T
AA Mutation	p.Ala539Ser(p.A539S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106066966:106066966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1822C>A
AA Mutation	p.Leu608Ile(p.L608I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067688:106067688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139881229
CDS Mutation	c.1100C>T
AA Mutation	p.Ser367Leu(p.S367L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067379:106067379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1409A>C
AA Mutation	p.Lys470Thr(p.K470T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106086864:106086864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.383T>C
AA Mutation	p.Ile128Thr(p.I128T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106066844:106066844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1944G>T
AA Mutation	p.Gln648His(p.Q648H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106138493:106138493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752539069
CDS Mutation	c.161G>A
AA Mutation	p.Arg54His(p.R54H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106086760:106086760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139582229
CDS Mutation	c.487G>A
AA Mutation	p.Val163Ile(p.V163I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067047:106067047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778868101
CDS Mutation	c.1741G>A
AA Mutation	p.Asp581Asn(p.D581N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106072762:106072762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661C>T
AA Mutation	p.Pro221Ser(p.P221S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067060:106067060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1728C>A
AA Mutation	p.Ser576Arg(p.S576R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067623:106067623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1165C>A
AA Mutation	p.Pro389Thr(p.P389T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067692:106067692(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096C>T
AA Mutation	p.Arg366Trp(p.R366W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106067914:106067914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546010292
CDS Mutation	c.874G>A
AA Mutation	p.Asp292Asn(p.D292N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106070818:106070818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753772566
CDS Mutation	c.788G>A
AA Mutation	p.Arg263Gln(p.R263Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106070884:106070884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.722T>C
AA Mutation	p.Val241Ala(p.V241A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000261402
Start	106138538:106138538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.116C>T
AA Mutation	p.Pro39Leu(p.P39L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106066841:106066841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1947C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106067219:106067219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1569C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106066925:106066925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1863G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106070847:106070847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.759C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106138549:106138549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106067048:106067048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs540753037
CDS Mutation	c.1740C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106067324:106067324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141601761
CDS Mutation	c.1464G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106067849:106067849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143829749
CDS Mutation	c.939C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261402
Start	106067268:106067268(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1520delC
AA Mutation	p.Pro507ArgfsTer6(p.P507Rfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261402
Start	106070886:106070887(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.719_720insAGGGC
AA Mutation	p.Val241GlyfsTer49(p.V241Gfs*49)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000261402
Start	106070772:106070772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.832+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000261402
Start	106086732:106086732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NUAK1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106086761:106086761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267603280
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106138549:106138549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.105G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261402
Start	106070847:106070847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.759C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000261402
Start	106067365:106067365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1423G>T
AA Mutation	p.Glu475Ter(p.E475*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript