Colon Cancer: Gene >> FGF12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000454309
Start	192408051:192408051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs551785451
CDS Mutation	c.173G>A
AA Mutation	p.Arg58His(p.R58H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000454309
Start	192408025:192408025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>A
AA Mutation	p.Glu67Lys(p.E67K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000454309
Start	192408091:192408091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766226672
CDS Mutation	c.133G>A
AA Mutation	p.Val45Ile(p.V45I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000454309
Start	192408094:192408094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.130C>G
AA Mutation	p.His44Asp(p.H44D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000454309
Start	192170577:192170577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768509717
CDS Mutation	c.494G>A
AA Mutation	p.Arg165His(p.R165H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000454309
Start	192408042:192408042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.182C>T
AA Mutation	p.Pro61Leu(p.P61L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454309
Start	192408065:192408065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.159C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454309
Start	192408092:192408092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752899505
CDS Mutation	c.132C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454309
Start	192408056:192408056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.168C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454309
Start	192144111:192144111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454309
Start	192170597:192170597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.474C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454309
Start	192360444:192360444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555759767
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000454309
Start	192408025:192408025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777885132
CDS Mutation	c.199G>T
AA Mutation	p.Glu67Ter(p.E67*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FGF12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000454309
Start	192170472:192170472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.599C>T
AA Mutation	p.Pro200Leu(p.P200L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000454309
Start	192408034:192408034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190C>T
AA Mutation	p.Arg64Trp(p.R64W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000454309
Start	192408111:192408111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113G>T
AA Mutation	p.Arg38Leu(p.R38L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000454309
Start	192144105:192144105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369115025
CDS Mutation	c.636G>A
Mutation Classification	Silent
Feature Type	Transcript