Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LAMB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209629900:209629900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969G>T
AA Mutation	p.Glu323Asp(p.E323D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209622651:209622651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2586G>T
AA Mutation	p.Gln862His(p.Q862H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209632635:209632635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770A>T
AA Mutation	p.Asp257Val(p.D257V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209632614:209632614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.791G>A
AA Mutation	p.Gly264Glu(p.G264E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209626899:209626899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144249951
CDS Mutation	c.1565G>A
AA Mutation	p.Arg522Gln(p.R522Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209623905:209623905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777788000
CDS Mutation	c.2072G>A
AA Mutation	p.Gly691Asp(p.G691D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209629911:209629911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958G>A
AA Mutation	p.Gly320Arg(p.G320R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209626956:209626956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202095584
CDS Mutation	c.1508G>A
AA Mutation	p.Arg503Gln(p.R503Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209615386:209615386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115712132
CDS Mutation	c.3404G>A
AA Mutation	p.Arg1135Gln(p.R1135Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209627552:209627552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1316G>A
AA Mutation	p.Arg439Gln(p.R439Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000356082
Start	209629923:209629923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.946T>C
AA Mutation	p.Cys316Arg(p.C316R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209634622:209634622(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389G>A
AA Mutation	p.Gly130Asp(p.G130D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209629769:209629769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772446912
CDS Mutation	c.1100G>A
AA Mutation	p.Arg367His(p.R367H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209625834:209625834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1790T>A
AA Mutation	p.Leu597Gln(p.L597Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209618497:209618497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2864A>G
AA Mutation	p.Asp955Gly(p.D955G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209632671:209632671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs114886812
CDS Mutation	c.734G>A
AA Mutation	p.Arg245His(p.R245H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209626900:209626900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775608853
CDS Mutation	c.1564C>T
AA Mutation	p.Arg522Trp(p.R522W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209629894:209629894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.975T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209628081:209628081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1242G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209616616:209616616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3237G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209615376:209615376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778923534
CDS Mutation	c.3414G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000356082
Start	209617481:209617481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3157C>T
AA Mutation	p.Gln1053Ter(p.Q1053*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LAMB3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209617941:209617941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751193145
CDS Mutation	c.3017G>A
AA Mutation	p.Arg1006His(p.R1006H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209629772:209629772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1097G>A
AA Mutation	p.Arg366Gln(p.R366Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209632696:209632696(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761752478
CDS Mutation	c.709G>A
AA Mutation	p.Ala237Thr(p.A237T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209615279:209615279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3511T>C
AA Mutation	p.Cys1171Arg(p.C1171R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356082
Start	209629920:209629920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949G>A
AA Mutation	p.Asp317Asn(p.D317N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356082
Start	209638601:209638601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript