Colon Cancer: Gene >> ADGRE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253673
Start	14654988:14654988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.571A>G
AA Mutation	p.Ser191Gly(p.S191G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000253673
Start	14638315:14638315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274C>T
AA Mutation	p.Ala425Val(p.A425V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000253673
Start	14641543:14641543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1124C>T
AA Mutation	p.Ala375Val(p.A375V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000253673
Start	14625599:14625599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1813G>T
AA Mutation	p.Val605Phe(p.V605F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000253673
Start	14625505:14625505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1907C>T
AA Mutation	p.Ser636Leu(p.S636L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000253673
Start	14625588:14625588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824A>T
AA Mutation	p.Gln608His(p.Q608H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253673
Start	14662054:14662054(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150826128
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253673
Start	14651173:14651173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253673
Start	14658522:14658522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.384C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253673
Start	14644252:14644252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253673
Start	14644267:14644267(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.891delC
AA Mutation	p.Ser298ValfsTer26(p.S298Vfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253673
Start	14647301:14647301(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.762delT
AA Mutation	p.Phe254LeufsTer12(p.F254Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000253673
Start	14638106:14638106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149254238
CDS Mutation	c.1483C>T
AA Mutation	p.Arg495Ter(p.R495*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADGRE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000253673
Start	14655132:14655132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427C>A
AA Mutation	p.Leu143Ile(p.L143I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253673
Start	14625564:14625564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147270469
CDS Mutation	c.1848C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253673
Start	14638179:14638179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201863044
CDS Mutation	c.1410C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253673
Start	14651173:14651173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000253673
Start	14632986:14632986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1578C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000253673
Start	14647301:14647301(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.762delT
AA Mutation	p.Phe254LeufsTer12(p.F254Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript