Colon Cancer: Gene >> CD53

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271324
Start	110897860:110897860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765838503
CDS Mutation	c.556G>A
AA Mutation	p.Gly186Arg(p.G186R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271324
Start	110892429:110892429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.148C>A
AA Mutation	p.Leu50Ile(p.L50I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271324
Start	110892505:110892505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224T>C
AA Mutation	p.Ile75Thr(p.I75T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271324
Start	110892455:110892455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529327509
CDS Mutation	c.174C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271324
Start	110892401:110892401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271324
Start	110891426:110891426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.18G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271324
Start	110892447:110892447(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.168delT
AA Mutation	p.Phe56LeufsTer10(p.F56Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CD53

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271324
Start	110896666:110896666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.437G>A
AA Mutation	p.Gly146Asp(p.G146D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271324
Start	110897820:110897820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768034243
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271324
Start	110892380:110892380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271324
Start	110894989:110894989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201211085
CDS Mutation	c.357C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000271324
Start	110896722:110896722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190729207
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Ter(p.R165*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript