Colon Cancer: Gene >> FGFR3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1806150:1806150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1936G>A
AA Mutation	p.Asp646Asn(p.D646N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1801630:1801630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.626A>G
AA Mutation	p.Gln209Arg(p.Q209R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1794040:1794040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106G>A
AA Mutation	p.Ala36Thr(p.A36T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1804449:1804449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370064407
CDS Mutation	c.1195C>T
AA Mutation	p.Arg399Cys(p.R399C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1806303:1806303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773089715
CDS Mutation	c.2006G>A
AA Mutation	p.Arg669Gln(p.R669Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1801460:1801460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539G>A
AA Mutation	p.Gly180Asp(p.G180D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1804843:1804843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1286C>T
AA Mutation	p.Ala429Val(p.A429V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1805455:1805455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144546453
CDS Mutation	c.1513G>A
AA Mutation	p.Val505Ile(p.V505I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1799401:1799401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.257G>A
AA Mutation	p.Arg86His(p.R86H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1807258:1807258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374547489
CDS Mutation	c.2417C>T
AA Mutation	p.Thr806Met(p.T806M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260795
Start	1806326:1806326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2029G>A
AA Mutation	p.Val677Ile(p.V677I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1804963:1804963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1406G>A
AA Mutation	p.Arg469Gln(p.R469Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1801501:1801501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580G>A
AA Mutation	p.Glu194Lys(p.E194K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000260795
Start	1806145:1806145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1931A>T
AA Mutation	p.Asn644Ile(p.N644I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260795
Start	1801416:1801416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260795
Start	1801935:1801935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776706695
CDS Mutation	c.840C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260795
Start	1806582:1806582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200872971
CDS Mutation	c.2067G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260795
Start	1803760:1803760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370530264
CDS Mutation	c.999C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260795
Start	1807259:1807259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779088139
CDS Mutation	c.2418G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260795
Start	1802007:1802007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.912C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260795
Start	1806600:1806600(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2088delC
AA Mutation	p.Gly697AlafsTer11(p.G697Afs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FGFR3

No Mutation Annotation!