Mutation

Primary Site >> Stomach Cancer

Gene >> ARHGAP29

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260526
Start	94173879:94173879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3776A>G
AA Mutation	p.Gln1259Arg(p.Q1259R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260526
Start	94174716:94174716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2939A>G
AA Mutation	p.Glu980Gly(p.E980G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260526
Start	94185041:94185041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748894382
CDS Mutation	c.1940G>A
AA Mutation	p.Arg647Gln(p.R647Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260526
Start	94202683:94202683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757995655
CDS Mutation	c.1004G>A
AA Mutation	p.Arg335His(p.R335H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000260526
Start	94202572:94202572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768915881
CDS Mutation	c.1115G>A
AA Mutation	p.Arg372Gln(p.R372Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260526
Start	94177612:94177612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2905G>T
AA Mutation	p.Asp969Tyr(p.D969Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260526
Start	94205082:94205082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.676G>T
AA Mutation	p.Val226Phe(p.V226F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000260526
Start	94174675:94174675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2980C>T
AA Mutation	p.Pro994Ser(p.P994S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260526
Start	94184872:94184872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2109G>T
AA Mutation	p.Gln703His(p.Q703H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000260526
Start	94201757:94201757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770096777
CDS Mutation	c.1244G>A
AA Mutation	p.Arg415Gln(p.R415Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260526
Start	94185459:94185459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1803T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260526
Start	94202575:94202575(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1112delA
AA Mutation	p.Lys371SerfsTer12(p.K371Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	13
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000260526
Start	94178019:94178045(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2603_2629delATTCAAATCAAGCACGCTTGGTAGAGT
AA Mutation	p.Tyr868_Glu876del(p.Y868_E876del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript