Colon Cancer: Gene >> FGG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336098
Start	154612561:154612561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>A
AA Mutation	p.Leu17Ile(p.L17I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336098
Start	154610112:154610112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487G>A
AA Mutation	p.Glu163Lys(p.E163K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336098
Start	154604918:154604918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1278C>G
AA Mutation	p.His426Gln(p.H426Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336098
Start	154612587:154612587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750711649
CDS Mutation	c.23G>A
AA Mutation	p.Arg8Gln(p.R8Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336098
Start	154606957:154606957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750162680
CDS Mutation	c.877G>A
AA Mutation	p.Val293Met(p.V293M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336098
Start	154610162:154610162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.437A>C
AA Mutation	p.Lys146Thr(p.K146T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000336098
Start	154609694:154609694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.602A>G
AA Mutation	p.Asn201Ser(p.N201S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336098
Start	154606709:154606709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766524002
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336098
Start	154609666:154609666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148688900
CDS Mutation	c.630C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336098
Start	154608609:154608609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336098
Start	154610083:154610083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336098
Start	154608474:154608474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.843C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336098
Start	154609750:154609750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.546T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000336098
Start	154612578:154612579(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.31_32insCATACTAAAAGAGAAAAAATACAGAAAT
AA Mutation	p.Ile11ThrfsTer3(p.I11Tfs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FGG

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336098
Start	154610116:154610116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript