Mutation

Primary Site >> Stomach Cancer

Gene >> DMBT1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122621114:122621114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199501579
CDS Mutation	c.4955G>A
AA Mutation	p.Arg1652Gln(p.R1652Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122643183:122643183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7027C>T
AA Mutation	p.Arg2343Trp(p.R2343W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122593593:122593593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2525G>C
AA Mutation	p.Ser842Thr(p.S842T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122586243:122586243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377302246
CDS Mutation	c.1643G>A
AA Mutation	p.Arg548Gln(p.R548Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122600076:122600076(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs191098913
CDS Mutation	c.3293G>A
AA Mutation	p.Arg1098Gln(p.R1098Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122586330:122586330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1730G>A
AA Mutation	p.Gly577Asp(p.G577D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122598998:122598998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768718263
CDS Mutation	c.3181C>T
AA Mutation	p.Arg1061Cys(p.R1061C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122637206:122637206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6449A>G
AA Mutation	p.Asp2150Gly(p.D2150G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122643232:122643232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147761345
CDS Mutation	c.7076G>A
AA Mutation	p.Arg2359His(p.R2359H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122631015:122631015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768251433
CDS Mutation	c.5693G>A
AA Mutation	p.Arg1898His(p.R1898H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122620280:122620280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4886C>T
AA Mutation	p.Ala1629Val(p.A1629V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122643126:122643126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372434439
CDS Mutation	c.6970G>A
AA Mutation	p.Val2324Met(p.V2324M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122586126:122586126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1526T>C
AA Mutation	p.Val509Ala(p.V509A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122598831:122598831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753951872
CDS Mutation	c.3014G>A
AA Mutation	p.Arg1005Gln(p.R1005Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122636161:122636161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201259183
CDS Mutation	c.6332G>A
AA Mutation	p.Arg2111Gln(p.R2111Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000338354
Start	122592506:122592506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2411G>C
AA Mutation	p.Gly804Ala(p.G804A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338354
Start	122577815:122577815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338354
Start	122599009:122599009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3192A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338354
Start	122631196:122631196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372991622
CDS Mutation	c.5874G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338354
Start	122631859:122631859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5964C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338354
Start	122579732:122579732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.834C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338354
Start	122637168:122637168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6411C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338354
Start	122643158:122643158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7002G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338354
Start	122588984:122588984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1824T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338354
Start	122643367:122643367(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.7217delC
AA Mutation	p.Pro2406HisfsTer24(p.P2406Hfs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	26
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000338354
Start	122637294:122637302(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.6539_6547delGCGGCACCT
AA Mutation	p.Cys2180_Thr2182del(p.C2180_T2182del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript