Colon Cancer: Gene >> FRMD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83309594:83309594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.868A>G
AA Mutation	p.Thr290Ala(p.T290A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83311905:83311905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767915126
CDS Mutation	c.755G>T
AA Mutation	p.Arg252Ile(p.R252I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83335604:83335604(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.508G>C
AA Mutation	p.Glu170Gln(p.E170Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83290707:83290707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372201657
CDS Mutation	c.1091G>A
AA Mutation	p.Arg364His(p.R364H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83313731:83313731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.613G>T
AA Mutation	p.Val205Phe(p.V205F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83335611:83335611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501G>T
AA Mutation	p.Glu167Asp(p.E167D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83313737:83313737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607C>T
AA Mutation	p.Pro203Ser(p.P203S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83290660:83290660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138C>A
AA Mutation	p.Leu380Met(p.L380M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83248199:83248199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778524664
CDS Mutation	c.1513C>T
AA Mutation	p.Arg505Cys(p.R505C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83538224:83538224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.8C>T
AA Mutation	p.Ala3Val(p.A3V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304195
Start	83313732:83313732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304195
Start	83313687:83313687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304195
Start	83335544:83335544(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.568delA
AA Mutation	p.Ile190Ter(p.I190*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304195
Start	83311950:83311950(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.710delT
AA Mutation	p.Leu237Ter(p.L237*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000304195
Start	83248408:83248409(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1303dupA
AA Mutation	p.Ile435AsnfsTer10(p.I435Nfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FRMD3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83343267:83343267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.395T>G
AA Mutation	p.Ile132Ser(p.I132S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83248326:83248326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1386G>T
AA Mutation	p.Glu462Asp(p.E462D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304195
Start	83299118:83299118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.995G>A
AA Mutation	p.Arg332Gln(p.R332Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304195
Start	83335623:83335623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746917345
CDS Mutation	c.489C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304195
Start	83335527:83335527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.585A>G
Mutation Classification	Silent
Feature Type	Transcript