Colon Cancer: Gene >> ADGRA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000412232
Start	37837769:37837769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377569553
CDS Mutation	c.2089G>A
AA Mutation	p.Val697Ile(p.V697I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000412232
Start	37841343:37841343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3005C>T
AA Mutation	p.Thr1002Met(p.T1002M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000412232
Start	37835560:37835560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757708388
CDS Mutation	c.1840G>A
AA Mutation	p.Val614Met(p.V614M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000412232
Start	37840773:37840773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142650653
CDS Mutation	c.2671G>A
AA Mutation	p.Ala891Thr(p.A891T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000412232
Start	37841175:37841175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2837C>T
AA Mutation	p.Ala946Val(p.A946V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000412232
Start	37837799:37837799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200831475
CDS Mutation	c.2119G>A
AA Mutation	p.Glu707Lys(p.E707K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000412232
Start	37841228:37841228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2890A>G
AA Mutation	p.Arg964Gly(p.R964G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000412232
Start	37814962:37814962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.333G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000412232
Start	37841356:37841356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3018G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000412232
Start	37797439:37797439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000412232
Start	37829506:37829506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000412232
Start	37829863:37829863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776402355
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412232
Start	37834087:37834087(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1573delG
AA Mutation	p.Ala525ProfsTer12(p.A525Pfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412232
Start	37841292:37841292(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2954delT
AA Mutation	p.Leu985ProfsTer2(p.L985Pfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000412232
Start	37835747:37835747(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2031delC
AA Mutation	p.Val678SerfsTer14(p.V678Sfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADGRA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000412232
Start	37835740:37835740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772222895
CDS Mutation	c.2020G>A
AA Mutation	p.Val674Met(p.V674M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000412232
Start	37837874:37837874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762378669
CDS Mutation	c.2194C>T
AA Mutation	p.Arg732Cys(p.R732C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000412232
Start	37814965:37814965(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.336delG
AA Mutation	p.Lys112AsnfsTer4(p.K112Nfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript