Mutation

Primary Site >> Stomach Cancer

Gene >> COL18A1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45487465:45487465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368967629
CDS Mutation	c.3097G>A
AA Mutation	p.Gly1033Arg(p.G1033R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45505173:45505173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4153C>T
AA Mutation	p.Pro1385Ser(p.P1385S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45468325:45468325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532978021
CDS Mutation	c.1435G>A
AA Mutation	p.Val479Ile(p.V479I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45512208:45512208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5075A>G
AA Mutation	p.His1692Arg(p.H1692R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45455546:45455546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.16T>C
AA Mutation	p.Cys6Arg(p.C6R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45480495:45480495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2672T>C
AA Mutation	p.Phe891Ser(p.F891S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45456165:45456165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635C>A
AA Mutation	p.Pro212Gln(p.P212Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45510107:45510107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200484625
CDS Mutation	c.4784G>A
AA Mutation	p.Arg1595Gln(p.R1595Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45512366:45512366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5233A>G
AA Mutation	p.Ile1745Val(p.I1745V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359759
Start	45494561:45494561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768453031
CDS Mutation	c.3614G>A
AA Mutation	p.Arg1205Gln(p.R1205Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45475481:45475481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1989C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45476416:45476416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45468717:45468717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1827C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45468321:45468321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372731688
CDS Mutation	c.1431C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45455587:45455587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45504478:45504478(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs564134000
CDS Mutation	c.4035C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45455836:45455836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777643778
CDS Mutation	c.306G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45455578:45455578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45480732:45480732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2730C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359759
Start	45490304:45490304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3234G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359759
Start	45505402:45505402(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.4307delC
AA Mutation	p.Pro1436LeufsTer10(p.P1436Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359759
Start	45468285:45468285(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1400delC
AA Mutation	p.Pro467ArgfsTer72(p.P467Rfs*72)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359759
Start	45496511:45496511(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3770delC
AA Mutation	p.Pro1257GlnfsTer67(p.P1257Qfs*67)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	24
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359759
Start	45480124:45480124(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2615delC
AA Mutation	p.Pro872GlnfsTer10(p.P872Qfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359759
Start	45468575:45468575(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1687delC
AA Mutation	p.His563ThrfsTer18(p.H563Tfs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript