Colon Cancer: Gene >> EPHA10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37723092:37723092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759710427
CDS Mutation	c.1909G>A
AA Mutation	p.Ala637Thr(p.A637T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37754348:37754348(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873G>T
AA Mutation	p.Lys291Asn(p.K291N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37721672:37721672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753810317
CDS Mutation	c.2134G>A
AA Mutation	p.Val712Ile(p.V712I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37762040:37762040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215G>A
AA Mutation	p.Arg72His(p.R72H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37727172:37727172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562741164
CDS Mutation	c.1702G>A
AA Mutation	p.Val568Ile(p.V568I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37719482:37719482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751281419
CDS Mutation	c.2688C>G
AA Mutation	p.Ile896Met(p.I896M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37761966:37761966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757411529
CDS Mutation	c.289C>T
AA Mutation	p.Arg97Cys(p.R97C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37720003:37720003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2468T>A
AA Mutation	p.Phe823Tyr(p.F823Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37762037:37762037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218C>T
AA Mutation	p.Thr73Met(p.T73M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37761785:37761785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470C>T
AA Mutation	p.Ala157Val(p.A157V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37761576:37761576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.679G>A
AA Mutation	p.Glu227Lys(p.E227K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37761813:37761813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139460043
CDS Mutation	c.442C>T
AA Mutation	p.Arg148Trp(p.R148W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373048
Start	37721727:37721727(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113277593
CDS Mutation	c.2079C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373048
Start	37731541:37731541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374180883
CDS Mutation	c.1533G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373048
Start	37721754:37721754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759686366
CDS Mutation	c.2052C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373048
Start	37718383:37718383(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3016delG
AA Mutation	p.Val1006CysfsTer82(p.V1006Cfs*82)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000373048
Start	37754215:37754215(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1006delC
AA Mutation	p.Arg336GlyfsTer13(p.R336Gfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000373048
Start	37719566:37719566(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2604delC
AA Mutation	p.Arg869GlyfsTer10(p.R869Gfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000373048
Start	37723168:37723168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56091464
CDS Mutation	c.1835-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> EPHA10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37761833:37761833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781544726
CDS Mutation	c.422G>A
AA Mutation	p.Arg141His(p.R141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373048
Start	37754287:37754287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.934G>A
AA Mutation	p.Ala312Thr(p.A312T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript