Colon Cancer: Gene >> TM7SF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26979904:26979904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762862395
CDS Mutation	c.1069G>A
AA Mutation	p.Val357Ile(p.V357I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26974078:26974078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1600C>A
AA Mutation	p.Pro534Thr(p.P534T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	27003381:27003381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.101A>C
AA Mutation	p.Glu34Ala(p.E34A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26980580:26980580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1022C>G
AA Mutation	p.Pro341Arg(p.P341R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26996774:26996774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.486C>G
AA Mutation	p.Ile162Met(p.I162M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26974123:26974123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1555T>G
AA Mutation	p.Leu519Val(p.L519V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26979901:26979901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759438192
CDS Mutation	c.1072G>A
AA Mutation	p.Gly358Ser(p.G358S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26976301:26976301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1246G>A
AA Mutation	p.Ala416Thr(p.A416T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26973984:26973984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1694G>A
AA Mutation	p.Arg565Lys(p.R565K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26975542:26975542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1404C>A
AA Mutation	p.Asn468Lys(p.N468K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343028
Start	26980573:26980573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1029G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343028
Start	26974031:26974031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1647A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343028
Start	26974148:26974148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372452992
CDS Mutation	c.1530G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343028
Start	26975500:26975500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1446T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000343028
Start	26999659:26999659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343028
Start	26974047:26974048(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1630_1631delAG
AA Mutation	p.Arg544AlafsTer9(p.R544Afs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000343028
Start	26975621:26975621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1325C>A
AA Mutation	p.Ser442Ter(p.S442*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TM7SF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000343028
Start	26995404:26995404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199925702
CDS Mutation	c.523G>A
AA Mutation	p.Val175Ile(p.V175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000343028
Start	26996768:26996768(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.492delT
AA Mutation	p.Phe164LeufsTer6(p.F164Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript