Colon Cancer: Gene >> TNKS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91813191:91813191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408G>T
AA Mutation	p.Lys136Asn(p.K136N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91819508:91819508(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584C>T
AA Mutation	p.Ala195Val(p.A195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91851219:91851219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2698A>G
AA Mutation	p.Thr900Ala(p.T900A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91857447:91857447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3011A>C
AA Mutation	p.Lys1004Thr(p.K1004T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91833976:91833976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1399T>G
AA Mutation	p.Phe467Val(p.F467V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91812991:91812991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.208C>T
AA Mutation	p.Arg70Trp(p.R70W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91819540:91819540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616G>A
AA Mutation	p.Ala206Thr(p.A206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91813168:91813168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.385C>T
AA Mutation	p.His129Tyr(p.H129Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91855630:91855630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2930G>A
AA Mutation	p.Arg977Gln(p.R977Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91833926:91833926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747895530
CDS Mutation	c.1349G>A
AA Mutation	p.Arg450His(p.R450H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91833932:91833932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1355T>G
AA Mutation	p.Leu452Arg(p.L452R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91819964:91819964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659G>C
AA Mutation	p.Gly220Ala(p.G220A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91828313:91828313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1011A>C
AA Mutation	p.Gln337His(p.Q337H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91833884:91833884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1307C>T
AA Mutation	p.Ser436Phe(p.S436F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371627
Start	91859541:91859541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371627
Start	91831145:91831145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1239T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371627
Start	91848535:91848535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2511A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371627
Start	91842189:91842189(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749004712
CDS Mutation	c.1865delA
AA Mutation	p.Asn622ThrfsTer29(p.N622Tfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371627
Start	91828344:91828344(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1047delA
AA Mutation	p.Lys349AsnfsTer8(p.K349Nfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371627
Start	91819496:91819496(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.577delA
AA Mutation	p.Met193Ter(p.M193*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000371627
Start	91855629:91855629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2929C>T
AA Mutation	p.Arg977Ter(p.R977*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000371627
Start	91845851:91845851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747817039
CDS Mutation	c.2269C>T
AA Mutation	p.Arg757Ter(p.R757*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000371627
Start	91833958:91833960(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1383_1385delTAT
AA Mutation	p.Ile462del(p.I462del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TNKS2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91862070:91862070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3353C>A
AA Mutation	p.Ser1118Tyr(p.S1118Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91828339:91828339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1037G>A
AA Mutation	p.Arg346Gln(p.R346Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371627
Start	91851253:91851253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2732A>C
AA Mutation	p.Glu911Ala(p.E911A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000371627
Start	91855629:91855629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2929C>T
AA Mutation	p.Arg977Ter(p.R977*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript