Colon Cancer: Gene >> TAOK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29987001:29987001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778268053
CDS Mutation	c.2729C>T
AA Mutation	p.Pro910Leu(p.P910L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29982756:29982756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.854G>A
AA Mutation	p.Arg285Gln(p.R285Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29987495:29987495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3223C>T
AA Mutation	p.Pro1075Ser(p.P1075S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29981715:29981715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710T>G
AA Mutation	p.Ile237Ser(p.I237S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29985313:29985313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1523C>T
AA Mutation	p.Ala508Val(p.A508V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29987466:29987466(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774325942
CDS Mutation	c.3194C>T
AA Mutation	p.Ala1065Val(p.A1065V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29979440:29979440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587C>T
AA Mutation	p.Ala196Val(p.A196V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29981873:29981873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778066032
CDS Mutation	c.764G>A
AA Mutation	p.Arg255Gln(p.R255Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29986574:29986574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2302G>T
AA Mutation	p.Gly768Cys(p.G768C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29985406:29985406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1616C>T
AA Mutation	p.Ala539Val(p.A539V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29985325:29985325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772408260
CDS Mutation	c.1535G>A
AA Mutation	p.Arg512Gln(p.R512Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29979457:29979457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604T>C
AA Mutation	p.Tyr202His(p.Y202H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29985424:29985424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755300621
CDS Mutation	c.1634G>A
AA Mutation	p.Arg545Gln(p.R545Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29982806:29982806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904C>T
AA Mutation	p.Arg302Trp(p.R302W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000308893
Start	29978995:29978995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.374A>G
AA Mutation	p.Glu125Gly(p.E125G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308893
Start	29983565:29983565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61739161
CDS Mutation	c.1323G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308893
Start	29986576:29986576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762567621
CDS Mutation	c.2304C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308893
Start	29987485:29987485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3213G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308893
Start	29983203:29983203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61738514
CDS Mutation	c.1131C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308893
Start	29983245:29983245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764182943
CDS Mutation	c.1173A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308893
Start	29987602:29987602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3330T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308893
Start	29982880:29982880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755169259
CDS Mutation	c.978C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308893
Start	29981889:29981889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000308893
Start	29987216:29987216(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2948delG
AA Mutation	p.Gly983ValfsTer50(p.G983Vfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000308893
Start	29987849:29987849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3577C>T
AA Mutation	p.Arg1193Ter(p.R1193*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000308893
Start	29985288:29985288(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1498C>T
AA Mutation	p.Arg500Ter(p.R500*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000308893
Start	29978972:29978972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TAOK2

No Mutation Annotation!