Colon Cancer: Gene >> ADAM33

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3669575:3669575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2303C>A
AA Mutation	p.Pro768His(p.P768H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3672617:3672617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321G>A
AA Mutation	p.Asp441Asn(p.D441N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3672169:3672169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769362525
CDS Mutation	c.1562C>T
AA Mutation	p.Thr521Met(p.T521M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3672256:3672256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1475C>A
AA Mutation	p.Ser492Tyr(p.S492Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3671121:3671121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2125A>T
AA Mutation	p.Ser709Cys(p.S709C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3669333:3669333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2370G>T
AA Mutation	p.Glu790Asp(p.E790D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3669592:3669592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2286C>G
AA Mutation	p.His762Gln(p.H762Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356518
Start	3673470:3673470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356518
Start	3674073:3674073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.729C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356518
Start	3674811:3674811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356518
Start	3672575:3672575(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1363delG
AA Mutation	p.Ala455ProfsTer14(p.A455Pfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000356518
Start	3675080:3675080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.280G>T
AA Mutation	p.Glu94Ter(p.E94*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM33

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356518
Start	3674132:3674132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.670T>A
AA Mutation	p.Leu224Met(p.L224M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356518
Start	3674564:3674564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.540C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356518
Start	3672588:3672588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350G>A
Mutation Classification	Silent
Feature Type	Transcript