Colon Cancer: Gene >> E2F8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19234751:19234751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.759T>G
AA Mutation	p.Phe253Leu(p.F253L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19224789:19224789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375220543
CDS Mutation	c.2473C>T
AA Mutation	p.Arg825Cys(p.R825C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19234446:19234446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755274793
CDS Mutation	c.842C>T
AA Mutation	p.Thr281Met(p.T281M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19234819:19234819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.691A>G
AA Mutation	p.Ile231Val(p.I231V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19229981:19229981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1366A>G
AA Mutation	p.Arg456Gly(p.R456G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19232365:19232365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.935T>A
AA Mutation	p.Ile312Asn(p.I312N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19229974:19229974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1373A>C
AA Mutation	p.Lys458Thr(p.K458T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19238080:19238080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68A>T
AA Mutation	p.Lys23Ile(p.K23I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19229494:19229494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1853A>G
AA Mutation	p.Lys618Arg(p.K618R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19234786:19234786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.724G>T
AA Mutation	p.Asp242Tyr(p.D242Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19224757:19224757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2505C>A
AA Mutation	p.Ser835Arg(p.S835R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19232363:19232363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937A>T
AA Mutation	p.Arg313Trp(p.R313W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000250024
Start	19235008:19235008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.502C>T
AA Mutation	p.His168Tyr(p.H168Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250024
Start	19225578:19225578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2064T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250024
Start	19225497:19225497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2145C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250024
Start	19238028:19238028(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250024
Start	19234904:19234904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs35243346
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250024
Start	19224769:19224769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2493C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000250024
Start	19237428:19237428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337C>T
AA Mutation	p.Arg113Ter(p.R113*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	stop_gained
Transcription ID	ENST00000250024
Start	19230724:19230724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177C>T
AA Mutation	p.Arg393Ter(p.R393*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000250024
Start	19229567:19229567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1780C>T
AA Mutation	p.Arg594Ter(p.R594*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000250024
Start	19224770:19224771(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.2491_2492insTTAAA
AA Mutation	p.Thr831IlefsTer21(p.T831Ifs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> E2F8

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250024
Start	19238124:19238124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24C>A
Mutation Classification	Silent
Feature Type	Transcript