Colon Cancer: Gene >> EPHA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93269529:93269529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1581T>G
AA Mutation	p.Ser527Arg(p.S527R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93243491:93243491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2932A>T
AA Mutation	p.Met978Leu(p.M978L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93358273:93358273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.971C>A
AA Mutation	p.Pro324Gln(p.P324Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93411050:93411050(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Ala95Thr(p.A95T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93410882:93410882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>A
AA Mutation	p.Ala151Thr(p.A151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93419253:93419253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89C>T
AA Mutation	p.Ala30Val(p.A30V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93358264:93358264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.980C>T
AA Mutation	p.Ala327Val(p.A327V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93272369:93272369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378G>A
AA Mutation	p.Glu460Lys(p.E460K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93246834:93246834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754119070
CDS Mutation	c.2684G>A
AA Mutation	p.Arg895Gln(p.R895Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93243439:93243439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755519422
CDS Mutation	c.2984G>A
AA Mutation	p.Gly995Asp(p.G995D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93357049:93357049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992C>A
AA Mutation	p.Pro331His(p.P331H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93259426:93259426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1852A>G
AA Mutation	p.Asn618Asp(p.N618D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93411077:93411077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770806616
CDS Mutation	c.256C>T
AA Mutation	p.Arg86Trp(p.R86W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93410634:93410634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.699A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93356945:93356945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1096A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93245386:93245386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2794C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93259454:93259454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93410955:93410955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93243534:93243534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767240586
CDS Mutation	c.2889G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93243510:93243510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774243019
CDS Mutation	c.2913T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93254764:93254764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781529358
CDS Mutation	c.2415C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93356967:93356967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1074G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93410970:93410970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537012893
CDS Mutation	c.363A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369303
Start	93419333:93419333(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.9delT
AA Mutation	p.Gln4LysfsTer97(p.Q4Kfs*97)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	stop_gained
Transcription ID	ENST00000369303
Start	93356855:93356855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186G>T
AA Mutation	p.Glu396Ter(p.E396*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	stop_gained
Transcription ID	ENST00000369303
Start	93246835:93246835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2683C>T
AA Mutation	p.Arg895Ter(p.R895*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	stop_gained
Transcription ID	ENST00000369303
Start	93269651:93269651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1459G>T
AA Mutation	p.Glu487Ter(p.E487*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	stop_gained
Transcription ID	ENST00000369303
Start	93245392:93245392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2788G>T
AA Mutation	p.Glu930Ter(p.E930*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EPHA7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93258234:93258234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1975G>T
AA Mutation	p.Asp659Tyr(p.D659Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93269564:93269564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1546C>T
AA Mutation	p.Arg516Trp(p.R516W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93410915:93410915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>A
AA Mutation	p.Glu140Lys(p.E140K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93245414:93245414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2766C>A
AA Mutation	p.Phe922Leu(p.F922L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93410719:93410719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.614G>T
AA Mutation	p.Cys205Phe(p.C205F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93358321:93358321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923C>A
AA Mutation	p.Ser308Tyr(p.S308Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000369303
Start	93410724:93410724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609G>T
AA Mutation	p.Lys203Asn(p.K203N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369303
Start	93246851:93246851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2667T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000369303
Start	93246835:93246835(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2683C>T
AA Mutation	p.Arg895Ter(p.R895*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000369303
Start	93246967:93246967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2551G>T
AA Mutation	p.Glu851Ter(p.E851*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript