Colon Cancer: Gene >> FLRT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14325938:14325938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1569A>C
AA Mutation	p.Lys523Asn(p.K523N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14326600:14326600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150799973
CDS Mutation	c.907C>T
AA Mutation	p.Arg303Cys(p.R303C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14327215:14327215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.292T>C
AA Mutation	p.Phe98Leu(p.F98L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14327005:14327005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502A>G
AA Mutation	p.Thr168Ala(p.T168A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14327369:14327369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.138T>G
AA Mutation	p.Asp46Glu(p.D46E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14327011:14327011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.496C>A
AA Mutation	p.Leu166Ile(p.L166I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14327497:14327497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142379846
CDS Mutation	c.10G>A
AA Mutation	p.Ala4Thr(p.A4T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14326407:14326407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1100C>A
AA Mutation	p.Thr367Asn(p.T367N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14326714:14326714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793A>G
AA Mutation	p.Asn265Asp(p.N265D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14326831:14326831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.676A>C
AA Mutation	p.Asn226His(p.N226H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14327265:14327265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.242A>C
AA Mutation	p.Asn81Thr(p.N81T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14325963:14325963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1544G>A
AA Mutation	p.Arg515Gln(p.R515Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14326074:14326074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1433G>A
AA Mutation	p.Cys478Tyr(p.C478Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341420
Start	14325815:14325815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1692A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341420
Start	14326232:14326232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1275C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341420
Start	14325773:14325773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1734T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341420
Start	14325882:14325883(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1624_1625insGGATAGAG
AA Mutation	p.Ile542ArgfsTer9(p.I542Rfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FLRT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14326853:14326853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654C>G
AA Mutation	p.Asp218Glu(p.D218E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14327127:14327127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380T>A
AA Mutation	p.Ile127Asn(p.I127N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341420
Start	14325606:14325606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763215176
CDS Mutation	c.1901G>A
AA Mutation	p.Arg634Gln(p.R634Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341420
Start	14326202:14326202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1305T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341420
Start	14327049:14327052(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.455_458delACAG
AA Mutation	p.Asp152AlafsTer25(p.D152Afs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript