Colon Cancer: Gene >> FGFR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38418369:38418369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1289C>T
AA Mutation	p.Ser430Phe(p.S430F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38419639:38419639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369059499
CDS Mutation	c.1178C>T
AA Mutation	p.Ser393Leu(p.S393L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000447712
Start	38428346:38428346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746094709
CDS Mutation	c.448C>T
AA Mutation	p.Pro150Ser(p.P150S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38428383:38428383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411G>T
AA Mutation	p.Glu137Asp(p.E137D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38413714:38413714(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781328162
CDS Mutation	c.2383G>A
AA Mutation	p.Val795Ile(p.V795I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38429808:38429808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.232C>T
AA Mutation	p.Arg78Cys(p.R78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38429702:38429702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338A>G
AA Mutation	p.Tyr113Cys(p.Y113C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38413946:38413946(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2264A>C
AA Mutation	p.Asp755Ala(p.D755A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38426215:38426215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.652G>A
AA Mutation	p.Asp218Asn(p.D218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38426235:38426235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632C>T
AA Mutation	p.Ala211Val(p.A211V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38418325:38418325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781608303
CDS Mutation	c.1333C>T
AA Mutation	p.Arg445Trp(p.R445W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38417356:38417356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1613T>C
AA Mutation	p.Ile538Thr(p.I538T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38421859:38421859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019C>T
AA Mutation	p.Thr340Met(p.T340M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447712
Start	38421807:38421807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746072842
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447712
Start	38424596:38424596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374583846
CDS Mutation	c.849G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447712
Start	38457387:38457387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773868899
CDS Mutation	c.60C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447712
Start	38429761:38429761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781034707
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000447712
Start	38427963:38427964(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.578dupA
AA Mutation	p.Asn193LysfsTer8(p.N193Kfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FGFR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447712
Start	38415895:38415895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1829G>A
AA Mutation	p.Gly610Asp(p.G610D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447712
Start	38417985:38417985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1437C>A
Mutation Classification	Silent
Feature Type	Transcript