Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LAMB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108092356:108092356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1531G>A
AA Mutation	p.Gly511Arg(p.G511R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108030974:108030974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4824A>C
AA Mutation	p.Glu1608Asp(p.E1608D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108037559:108037559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200882131
CDS Mutation	c.4508C>T
AA Mutation	p.Ala1503Val(p.A1503V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000205386
Start	108052099:108052099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778024891
CDS Mutation	c.3914C>T
AA Mutation	p.Ala1305Val(p.A1305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108107741:108107741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481A>G
AA Mutation	p.Lys161Glu(p.K161E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108106538:108106538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626T>G
AA Mutation	p.Ile209Ser(p.I209S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108048048:108048048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4186G>T
AA Mutation	p.Gly1396Cys(p.G1396C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108091654:108091654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1673C>T
AA Mutation	p.Ala558Val(p.A558V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108105846:108105846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751482652
CDS Mutation	c.841C>T
AA Mutation	p.Arg281Trp(p.R281W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108068072:108068072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2390G>T
AA Mutation	p.Arg797Leu(p.R797L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108116119:108116119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.77G>T
AA Mutation	p.Gly26Val(p.G26V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108079698:108079698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1790G>A
AA Mutation	p.Gly597Glu(p.G597E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108105927:108105927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.760T>C
AA Mutation	p.Tyr254His(p.Y254H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000205386
Start	108057927:108057927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3284T>G
AA Mutation	p.Leu1095Arg(p.L1095R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108105903:108105903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766405251
CDS Mutation	c.784C>T
AA Mutation	p.Arg262Trp(p.R262W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108066377:108066377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2670C>A
AA Mutation	p.Asn890Lys(p.N890K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108055812:108055812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755935994
CDS Mutation	c.3575C>T
AA Mutation	p.Ala1192Val(p.A1192V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000205386
Start	108057832:108057832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769773184
CDS Mutation	c.3379C>T
AA Mutation	p.Pro1127Ser(p.P1127S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108111847:108111847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.292C>A
AA Mutation	p.Pro98Thr(p.P98T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108037550:108037550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4517T>G
AA Mutation	p.Val1506Gly(p.V1506G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108062933:108062933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3123C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108077004:108077004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2064C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108103093:108103093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1131C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108103153:108103153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373050835
CDS Mutation	c.1071C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108037486:108037486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4581A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108103171:108103171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108098545:108098545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108063822:108063822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3000C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108063966:108063966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2856C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108103051:108103051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768213293
CDS Mutation	c.1173G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	stop_gained
Transcription ID	ENST00000205386
Start	108107763:108107763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.459G>A
AA Mutation	p.Trp153Ter(p.W153*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000205386
Start	108107630:108107630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> LAMB4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108106014:108106014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673A>G
AA Mutation	p.Asn225Asp(p.N225D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108047945:108047945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4289G>A
AA Mutation	p.Arg1430His(p.R1430H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108049473:108049473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3975T>G
AA Mutation	p.Ile1325Met(p.I1325M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108047987:108047987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4247C>A
AA Mutation	p.Thr1416Lys(p.T1416K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108055732:108055732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3655G>T
AA Mutation	p.Asp1219Tyr(p.D1219Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000205386
Start	108103106:108103106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118G>A
AA Mutation	p.Arg373His(p.R373H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108066395:108066395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2652C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108077040:108077040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2028C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108043867:108043867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4356C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000205386
Start	108103090:108103090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000205386
Start	108065904:108065904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2694C>A
AA Mutation	p.Tyr898Ter(p.Y898*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript