Mutation

Primary Site >> Stomach Cancer

Gene >> DDR1

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000324771
Start	30898073:30898073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2217C>G
AA Mutation	p.Ser739Arg(p.S739R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30891098:30891098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.543G>T
AA Mutation	p.Glu181Asp(p.E181D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30890998:30890998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.443A>G
AA Mutation	p.Glu148Gly(p.E148G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30895472:30895472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1582G>A
AA Mutation	p.Gly528Ser(p.G528S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30893110:30893110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371183562
CDS Mutation	c.1142C>T
AA Mutation	p.Pro381Leu(p.P381L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30895487:30895487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1597G>A
AA Mutation	p.Ala533Thr(p.A533T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30888772:30888772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.43G>T
AA Mutation	p.Val15Leu(p.V15L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30892110:30892110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>T
AA Mutation	p.Trp258Cys(p.W258C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30898159:30898159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2303C>T
AA Mutation	p.Ala768Val(p.A768V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30897557:30897557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2176G>C
AA Mutation	p.Ala726Pro(p.A726P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30899184:30899184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776556090
CDS Mutation	c.2630C>T
AA Mutation	p.Pro877Leu(p.P877L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30895488:30895488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1598C>T
AA Mutation	p.Ala533Val(p.A533V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000324771
Start	30898955:30898955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2519G>C
AA Mutation	p.Cys840Ser(p.C840S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324771
Start	30892319:30892319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.876G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324771
Start	30893408:30893408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1332C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324771
Start	30898163:30898163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748824831
CDS Mutation	c.2307G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324771
Start	30893390:30893390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1314C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324771
Start	30895474:30895474(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1590delC
AA Mutation	p.Thr531HisfsTer122(p.T531Hfs*122)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324771
Start	30891024:30891024(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.474delC
AA Mutation	p.Met159TrpfsTer16(p.M159Wfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324771
Start	30896794:30896794(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1803delC
AA Mutation	p.Arg602GlufsTer51(p.R602Efs*51)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript