Colon Cancer: Gene >> PFAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8269206:8269206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3959C>T
AA Mutation	p.Ser1320Phe(p.S1320F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8265081:8265081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780319540
CDS Mutation	c.2236G>A
AA Mutation	p.Glu746Lys(p.E746K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8254249:8254249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226G>A
AA Mutation	p.Glu76Lys(p.E76K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8263849:8263849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1704G>T
AA Mutation	p.Arg568Ser(p.R568S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8266878:8266878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2947G>A
AA Mutation	p.Glu983Lys(p.E983K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8267630:8267630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3347G>A
AA Mutation	p.Gly1116Asp(p.G1116D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8266257:8266257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2725G>A
AA Mutation	p.Asp909Asn(p.D909N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8265459:8265459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779350437
CDS Mutation	c.2452C>T
AA Mutation	p.Arg818Trp(p.R818W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8265456:8265456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754015723
CDS Mutation	c.2449G>A
AA Mutation	p.Val817Met(p.V817M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8265601:8265601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2507C>T
AA Mutation	p.Ala836Val(p.A836V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8266846:8266846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2915G>A
AA Mutation	p.Gly972Asp(p.G972D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8268637:8268637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3487C>G
AA Mutation	p.Leu1163Val(p.L1163V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8255547:8255547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430A>G
AA Mutation	p.Thr144Ala(p.T144A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8253956:8253956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.19T>G
AA Mutation	p.Phe7Val(p.F7V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8269037:8269037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537007406
CDS Mutation	c.3790G>A
AA Mutation	p.Gly1264Arg(p.G1264R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314666
Start	8263915:8263915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1770C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314666
Start	8255818:8255818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367964525
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314666
Start	8266880:8266880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2949G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314666
Start	8254230:8254230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.207G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000314666
Start	8264259:8264259(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1843delG
AA Mutation	p.Asp615MetfsTer45(p.D615Mfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PFAS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8255871:8255871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641C>A
AA Mutation	p.Pro214Gln(p.P214Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314666
Start	8255556:8255556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.439G>A
AA Mutation	p.Asp147Asn(p.D147N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript