Colon Cancer: Gene >> TYK2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10350929:10350929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3469T>A
AA Mutation	p.Ser1157Thr(p.S1157T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10368377:10368377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.235G>A
AA Mutation	p.Ala79Thr(p.A79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10352933:10352933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3193G>T
AA Mutation	p.Val1065Leu(p.V1065L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10378292:10378292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201283990
CDS Mutation	c.115G>A
AA Mutation	p.Gly39Ser(p.G39S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10358030:10358030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368361707
CDS Mutation	c.2284G>A
AA Mutation	p.Val762Met(p.V762M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10362158:10362158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776940518
CDS Mutation	c.1693C>T
AA Mutation	p.Arg565Trp(p.R565W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10362353:10362353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755791270
CDS Mutation	c.1580G>A
AA Mutation	p.Arg527Gln(p.R527Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10354543:10354543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2684G>A
AA Mutation	p.Arg895His(p.R895H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10353559:10353559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2996A>G
AA Mutation	p.Gln999Arg(p.Q999R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10350866:10350866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3532G>T
AA Mutation	p.Gly1178Cys(p.G1178C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10358119:10358119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2195A>G
AA Mutation	p.His732Arg(p.H732R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000264818
Start	10352465:10352465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3287C>T
AA Mutation	p.Thr1096Met(p.T1096M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10358097:10358097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2217C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10354520:10354520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2707C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10357914:10357914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758779015
CDS Mutation	c.2316G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264818
Start	10366464:10366464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147934502
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264818
Start	10352437:10352437(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3315delC
AA Mutation	p.Thr1106ArgfsTer7(p.T1106Rfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000264818
Start	10361904:10361904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749285570
CDS Mutation	c.1825C>T
AA Mutation	p.Arg609Ter(p.R609*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264818
Start	10366441:10366442(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.604dupC
AA Mutation	p.Leu202ProfsTer105(p.L202Pfs*105)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TYK2

No Mutation Annotation!