Colon Cancer: Gene >> TSHR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81143781:81143781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757875222
CDS Mutation	c.1723G>A
AA Mutation	p.Glu575Lys(p.E575K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81139783:81139783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.797C>T
AA Mutation	p.Ser266Phe(p.S266F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81143545:81143545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1487C>T
AA Mutation	p.Thr496Met(p.T496M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81143916:81143916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1858A>G
AA Mutation	p.Thr620Ala(p.T620A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81143400:81143400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201889708
CDS Mutation	c.1342G>A
AA Mutation	p.Val448Ile(p.V448I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81143202:81143202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1144G>T
AA Mutation	p.Asp382Tyr(p.D382Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81143092:81143092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1034A>C
AA Mutation	p.Asp345Ala(p.D345A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81142987:81142987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139286618
CDS Mutation	c.929G>A
AA Mutation	p.Arg310His(p.R310H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81144297:81144297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2239C>A
AA Mutation	p.Leu747Ile(p.L747I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81144060:81144060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2002C>A
AA Mutation	p.Pro668Thr(p.P668T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81143841:81143841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142632518
CDS Mutation	c.1783G>A
AA Mutation	p.Val595Ile(p.V595I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541158
Start	81091084:81091084(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.408T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541158
Start	81143780:81143780(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369247508
CDS Mutation	c.1722C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541158
Start	80955830:80955830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541158
Start	81139817:81139817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541158
Start	81143159:81143159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000541158
Start	81144188:81144189(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2130_2131insAGTTAAGTGGATA
AA Mutation	p.Val711SerfsTer2(p.V711Sfs*2)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TSHR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81139702:81139702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716C>T
AA Mutation	p.Thr239Ile(p.T239I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000541158
Start	81092551:81092551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488A>T
AA Mutation	p.Tyr163Phe(p.Y163F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541158
Start	81068272:81068272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000541158
Start	81139856:81139856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.870G>A
Mutation Classification	Silent
Feature Type	Transcript