Colon Cancer: Gene >> SIX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60723618:60723618(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457G>C
AA Mutation	p.Ala153Pro(p.A153P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60713584:60713584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2169G>T
AA Mutation	p.Glu723Asp(p.E723D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60719925:60719925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384G>A
AA Mutation	p.Ala462Thr(p.A462T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60723659:60723659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.416G>A
AA Mutation	p.Ser139Asn(p.S139N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60713586:60713586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2167G>A
AA Mutation	p.Glu723Lys(p.E723K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60720014:60720014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1295C>G
AA Mutation	p.Thr432Ser(p.T432S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60713894:60713894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1859T>C
AA Mutation	p.Phe620Ser(p.F620S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60719781:60719781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1528G>A
AA Mutation	p.Val510Met(p.V510M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60723704:60723704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.371G>A
AA Mutation	p.Gly124Asp(p.G124D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60713961:60713961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1792A>C
AA Mutation	p.Asn598His(p.N598H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60719803:60719803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506C>A
AA Mutation	p.Phe502Leu(p.F502L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60720206:60720206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369624724
CDS Mutation	c.1103C>A
AA Mutation	p.Ser368Tyr(p.S368Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60719936:60719936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1373T>C
AA Mutation	p.Ile458Thr(p.I458T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60719813:60719813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1496G>A
AA Mutation	p.Ser499Asn(p.S499N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216513
Start	60719809:60719809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1500T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216513
Start	60713577:60713577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2176T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216513
Start	60713485:60713485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2268T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216513
Start	60713695:60713695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2058G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216513
Start	60713683:60713683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2070T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000216513
Start	60723704:60723704(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.371delG
AA Mutation	p.Gly124AlafsTer26(p.G124Afs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SIX4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60720289:60720289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020G>T
AA Mutation	p.Lys340Asn(p.K340N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60714122:60714122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1631T>C
AA Mutation	p.Phe544Ser(p.F544S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60719915:60719915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1394A>G
AA Mutation	p.Asp465Gly(p.D465G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000216513
Start	60713567:60713567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2186C>T
AA Mutation	p.Ser729Phe(p.S729F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216513
Start	60713956:60713956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1797C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216513
Start	60720367:60720367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.942T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000216513
Start	60720199:60720199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110T>C
Mutation Classification	Silent
Feature Type	Transcript