Colon Cancer: Gene >> ADAM11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000200557
Start	44776172:44776172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1531G>A
AA Mutation	p.Asp511Asn(p.D511N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000200557
Start	44778170:44778170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2204T>C
AA Mutation	p.Ile735Thr(p.I735T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000200557
Start	44776193:44776193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1552G>C
AA Mutation	p.Gly518Arg(p.G518R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000200557
Start	44778227:44778227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762803709
CDS Mutation	c.2261C>T
AA Mutation	p.Thr754Met(p.T754M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000200557
Start	44778160:44778160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2194G>A
AA Mutation	p.Gly732Ser(p.G732S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000200557
Start	44772327:44772327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604G>A
AA Mutation	p.Glu202Lys(p.E202K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000200557
Start	44777798:44777798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2005G>A
AA Mutation	p.Ala669Thr(p.A669T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000200557
Start	44772416:44772416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628C>T
AA Mutation	p.Pro210Ser(p.P210S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000200557
Start	44775279:44775279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1288G>T
AA Mutation	p.Gly430Cys(p.G430C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000200557
Start	44778228:44778228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575543165
CDS Mutation	c.2262G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200557
Start	44777537:44777537(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1840delG
AA Mutation	p.Asp614ThrfsTer33(p.D614Tfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000200557
Start	44774337:44774337(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1040delG
AA Mutation	p.Gly347AlafsTer11(p.G347Afs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ADAM11

Mutation ID	1
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000200557
Start	44776897:44776897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1618-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript