Colon Cancer: Gene >> AMOTL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000422605
Start	134359442:134359442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140029062
CDS Mutation	c.1945C>T
AA Mutation	p.Arg649Cys(p.R649C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000422605
Start	134365885:134365885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139298691
CDS Mutation	c.1211G>A
AA Mutation	p.Arg404His(p.R404H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000422605
Start	134367715:134367715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.823C>T
AA Mutation	p.Pro275Ser(p.P275S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000422605
Start	134358644:134358644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2177G>T
AA Mutation	p.Gly726Val(p.G726V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000422605
Start	134366358:134366358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148721825
CDS Mutation	c.1111G>A
AA Mutation	p.Ala371Thr(p.A371T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000422605
Start	134359400:134359400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781488712
CDS Mutation	c.1987C>T
AA Mutation	p.Arg663Trp(p.R663W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422605
Start	134360297:134360297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758990000
CDS Mutation	c.1692C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422605
Start	134367586:134367586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.952C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000422605
Start	134357708:134357708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2337C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000422605
Start	134370835:134370835(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs756346527
CDS Mutation	c.599delC
AA Mutation	p.Pro200LeufsTer19(p.P200Lfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> AMOTL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000422605
Start	134366418:134366418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1051G>A
AA Mutation	p.Glu351Lys(p.E351K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript