Colon Cancer: Gene >> EPHA1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000275815
Start	143397322:143397322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs34178823
CDS Mutation	c.1753G>A
AA Mutation	p.Ala585Thr(p.A585T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000275815
Start	143401548:143401548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.208C>T
AA Mutation	p.Pro70Ser(p.P70S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000275815
Start	143398756:143398756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140236236
CDS Mutation	c.1181C>T
AA Mutation	p.Pro394Leu(p.P394L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000275815
Start	143393776:143393776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2591C>T
AA Mutation	p.Ala864Val(p.A864V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000275815
Start	143399909:143399909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577G>A
AA Mutation	p.Ala193Thr(p.A193T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000275815
Start	143401555:143401555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.201G>T
AA Mutation	p.Gln67His(p.Q67H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000275815
Start	143401343:143401343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190437539
CDS Mutation	c.413G>A
AA Mutation	p.Arg138Gln(p.R138Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000275815
Start	143399822:143399822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756665403
CDS Mutation	c.664G>A
AA Mutation	p.Ala222Thr(p.A222T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000275815
Start	143398332:143398332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144470322
CDS Mutation	c.1453G>A
AA Mutation	p.Val485Met(p.V485M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275815
Start	143401351:143401351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.405T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275815
Start	143398935:143398935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373641317
CDS Mutation	c.1002G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275815
Start	143399262:143399262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.987C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275815
Start	143394847:143394847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2313T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275815
Start	143398746:143398746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1191G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275815
Start	143394886:143394886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755323612
CDS Mutation	c.2274T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000275815
Start	143395484:143395484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112723648
CDS Mutation	c.1918C>T
AA Mutation	p.Arg640Ter(p.R640*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> EPHA1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275815
Start	143399763:143399763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275815
Start	143395329:143395329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2073C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000275815
Start	143398375:143398375(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1410C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000275815
Start	143400017:143400017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141528182
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Ter(p.R157*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript