Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CD72

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259633
Start	35612912:35612912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770G>A
AA Mutation	p.Ser257Asn(p.S257N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000259633
Start	35610723:35610723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.981G>C
AA Mutation	p.Lys327Asn(p.K327N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000259633
Start	35611905:35611905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.849C>A
AA Mutation	p.Phe283Leu(p.F283L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000259633
Start	35611810:35611810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770122832
CDS Mutation	c.944G>A
AA Mutation	p.Arg315His(p.R315H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000259633
Start	35612865:35612865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817G>T
AA Mutation	p.Glu273Ter(p.E273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000259633
Start	35616617:35616618(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.308_334dupCCTGCCTGCTGTTAGGAGTGACCGCCA
AA Mutation	p.Thr103_Ala111dup(p.T103_A111dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CD72

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259633
Start	35610746:35610746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958G>A
AA Mutation	p.Ala320Thr(p.A320T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259633
Start	35618096:35618096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.108A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259633
Start	35616247:35616247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.384G>A
Mutation Classification	Silent
Feature Type	Transcript