Mutation

Primary Site >> Stomach Cancer

Gene >> ARAF

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377045
Start	47571012:47571012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1686G>T
AA Mutation	p.Gln562His(p.Q562H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377045
Start	47563327:47563327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.198G>C
AA Mutation	p.Lys66Asn(p.K66N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47564805:47564805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199527940
CDS Mutation	c.209C>T
AA Mutation	p.Thr70Met(p.T70M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47570996:47570996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1670G>A
AA Mutation	p.Arg557Gln(p.R557Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47569913:47569913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1440G>T
AA Mutation	p.Met480Ile(p.M480I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377045
Start	47568773:47568773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1132T>C
AA Mutation	p.Phe378Leu(p.F378L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377045
Start	47564863:47564863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.267G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377045
Start	47567316:47567316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748240627
CDS Mutation	c.960G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377045
Start	47565309:47565309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs56202823
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377045
Start	47566695:47566695(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.619delC
AA Mutation	p.Leu207TyrfsTer85(p.L207Yfs*85)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377045
Start	47567016:47567016(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.763delC
AA Mutation	p.Arg255GlyfsTer37(p.R255Gfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000377045
Start	47569914:47569914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1441C>T
AA Mutation	p.Gln481Ter(p.Q481*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000377045
Start	47567133:47567133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.873+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	14
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000377045
Start	47566722:47566727(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.644_649delCTCCCA
AA Mutation	p.Thr215_Pro216del(p.T215_P216del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript