Colon Cancer: Gene >> PHEX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22047077:22047077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215T>G
AA Mutation	p.Leu72Arg(p.L72R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22093986:22093986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.736C>T
AA Mutation	p.Arg246Trp(p.R246W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22077662:22077662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623T>C
AA Mutation	p.Val208Ala(p.V208A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22114506:22114506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1222A>C
AA Mutation	p.Asn408His(p.N408H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000379374
Start	22168387:22168387(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1480G>T
AA Mutation	p.Ala494Ser(p.A494S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22093992:22093992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.742G>A
AA Mutation	p.Ala248Thr(p.A248T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22099096:22099096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761575825
CDS Mutation	c.1024C>T
AA Mutation	p.Arg342Cys(p.R342C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22133567:22133567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1347G>T
AA Mutation	p.Met449Ile(p.M449I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22221628:22221628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1784A>C
AA Mutation	p.Lys595Thr(p.K595T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22076426:22076426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>A
AA Mutation	p.Glu130Lys(p.E130K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22076450:22076450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>A
AA Mutation	p.Leu138Ile(p.L138I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22033091:22033091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.86G>A
AA Mutation	p.Gly29Asp(p.G29D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22077623:22077623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748279755
CDS Mutation	c.584G>A
AA Mutation	p.Arg195His(p.R195H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379374
Start	22094045:22094045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379374
Start	22033029:22033029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379374
Start	22114556:22114556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1272T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PHEX

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22033064:22033064(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59G>A
AA Mutation	p.Arg20Gln(p.R20Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22047148:22047148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149168023
CDS Mutation	c.286G>A
AA Mutation	p.Glu96Lys(p.E96K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22178322:22178322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778363445
CDS Mutation	c.1532A>C
AA Mutation	p.Lys511Thr(p.K511T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000379374
Start	22226489:22226489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1946G>A
AA Mutation	p.Gly649Asp(p.G649D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379374
Start	22190456:22190456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1599T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000379374
Start	22038530:22038530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.180C>T
Mutation Classification	Silent
Feature Type	Transcript