Colon Cancer: Gene >> FGF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334134
Start	69810606:69810606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782226740
CDS Mutation	c.419C>T
AA Mutation	p.Thr140Met(p.T140M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334134
Start	69810594:69810594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781807006
CDS Mutation	c.431G>A
AA Mutation	p.Arg144His(p.R144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334134
Start	69810373:69810373(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	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334134
Start	69810437:69810437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.588T>G
AA Mutation	p.Ser196Arg(p.S196R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334134
Start	69810438:69810438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.587G>T
AA Mutation	p.Ser196Ile(p.S196I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334134
Start	69810621:69810621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199801193
CDS Mutation	c.404G>A
AA Mutation	p.Arg135Gln(p.R135Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334134
Start	69810395:69810395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334134
Start	69810353:69810353(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375708730
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> FGF3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334134
Start	69816333:69816333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150581924
CDS Mutation	c.311G>A
AA Mutation	p.Arg104Gln(p.R104Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334134
Start	69810689:69810689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148729466
CDS Mutation	c.336C>T
Mutation Classification	Silent
Feature Type	Transcript