Mutation

Primary Site >> Stomach Cancer

Gene >> AR

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67686088:67686088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754201976
CDS Mutation	c.1847G>A
AA Mutation	p.Arg616His(p.R616H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545876:67545876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.730T>G
AA Mutation	p.Ser244Ala(p.S244A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545856:67545856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710A>G
AA Mutation	p.Lys237Arg(p.K237R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374690
Start	67686010:67686010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1769G>A
AA Mutation	p.Gly590Glu(p.G590E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545984:67545984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.838C>T
AA Mutation	p.Arg280Cys(p.R280C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67722962:67722962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750930905
CDS Mutation	c.2585A>G
AA Mutation	p.Lys862Arg(p.K862R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67721954:67721954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2440T>G
AA Mutation	p.Phe814Val(p.F814V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67546041:67546041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.895G>A
AA Mutation	p.Ala299Thr(p.A299T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67686046:67686046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1805G>A
AA Mutation	p.Cys602Tyr(p.C602Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67711627:67711627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2111G>A
AA Mutation	p.Ser704Asn(p.S704N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67721954:67721954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2440T>C
AA Mutation	p.Phe814Leu(p.F814L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67643281:67643281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1642T>G
AA Mutation	p.Leu548Val(p.L548V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67721941:67721941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2427A>C
AA Mutation	p.Lys809Asn(p.K809N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67721838:67721838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137852572
CDS Mutation	c.2324G>A
AA Mutation	p.Arg775His(p.R775H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67545954:67545954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808G>A
AA Mutation	p.Ala270Thr(p.A270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67721847:67721847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2333A>C
AA Mutation	p.Lys778Thr(p.K778T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67546023:67546023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877T>C
AA Mutation	p.Ser293Pro(p.S293P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67722924:67722924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2547T>G
AA Mutation	p.Asn849Lys(p.N849K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000374690
Start	67546311:67546311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165C>A
AA Mutation	p.Leu389Met(p.L389M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67717491:67717491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2187A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67546043:67546043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67546742:67546742(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1596C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67546040:67546040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.894C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67545803:67545803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.657T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67546400:67546400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1254T>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67545239:67545239(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.93C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374690
Start	67722945:67722945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2568C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374690
Start	67546736:67546737(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1591dupT
AA Mutation	p.Tyr531LeufsTer21(p.Y531Lfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript