Mutation

Primary Site >> Stomach Cancer

Gene >> RNF6

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214323:26214323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1559T>C
AA Mutation	p.Leu520Pro(p.L520P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214164:26214164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1718A>C
AA Mutation	p.Asn573Thr(p.N573T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26215127:26215127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774282689
CDS Mutation	c.755G>A
AA Mutation	p.Arg252His(p.R252H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214123:26214123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1759C>T
AA Mutation	p.Arg587Cys(p.R587C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214953:26214953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929G>A
AA Mutation	p.Arg310Gln(p.R310Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214849:26214849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033G>T
AA Mutation	p.Gly345Cys(p.G345C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26218576:26218576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224G>A
AA Mutation	p.Arg75Gln(p.R75Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26214806:26214806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745325624
CDS Mutation	c.1076G>A
AA Mutation	p.Arg359His(p.R359H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000346166
Start	26213831:26213831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2051A>T
AA Mutation	p.Asn684Ile(p.N684I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346166
Start	26214104:26214104(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1778delT
AA Mutation	p.Leu593TyrfsTer2(p.L593Yfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000346166
Start	26214103:26214104(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1778dupT
AA Mutation	p.Leu593PhefsTer4(p.L593Ffs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript