Mutation

Primary Site >> Stomach Cancer

Gene >> COLEC12

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	348092:348092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253G>T
AA Mutation	p.Ala85Ser(p.A85S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	347104:347104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201197346
CDS Mutation	c.518C>T
AA Mutation	p.Ala173Val(p.A173V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	348100:348100(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245A>C
AA Mutation	p.Lys82Thr(p.K82T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	335158:335158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1400G>A
AA Mutation	p.Gly467Glu(p.G467E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000400256
Start	480755:480755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.10G>A
AA Mutation	p.Asp4Asn(p.D4N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	347270:347270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.352C>A
AA Mutation	p.Leu118Ile(p.L118I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	348068:348068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277T>A
AA Mutation	p.Leu93Ile(p.L93I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	347267:347267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs555229244
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Cys(p.R119C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	331713:331713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373227938
CDS Mutation	c.2018G>A
AA Mutation	p.Arg673His(p.R673H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	347195:347195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757520445
CDS Mutation	c.427G>A
AA Mutation	p.Gly143Arg(p.G143R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	334825:334825(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1733G>C
AA Mutation	p.Gly578Ala(p.G578A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	321787:321787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138304922
CDS Mutation	c.2084C>T
AA Mutation	p.Pro695Leu(p.P695L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	333120:333120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1840T>G
AA Mutation	p.Phe614Val(p.F614V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	480739:480739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26A>T
AA Mutation	p.Glu9Val(p.E9V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000400256
Start	346537:346537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1085G>T
AA Mutation	p.Ser362Ile(p.S362I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400256
Start	346722:346722(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781630091
CDS Mutation	c.900C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400256
Start	346509:346509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1113C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400256
Start	346782:346782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370741108
CDS Mutation	c.840C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400256
Start	335079:335079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770196943
CDS Mutation	c.1479C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400256
Start	334972:334972(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs755024639
CDS Mutation	c.1586delC
AA Mutation	p.Pro529ArgfsTer117(p.P529Rfs*117)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400256
Start	331763:331763(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1968delA
AA Mutation	p.Lys656AsnfsTer4(p.K656Nfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000400256
Start	347237:347237(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.385delA
AA Mutation	p.Thr129ProfsTer25(p.T129Pfs*25)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	stop_gained
Transcription ID	ENST00000400256
Start	357517:357517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.64C>T
AA Mutation	p.Gln22Ter(p.Q22*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript