Mutation

Primary Site >> Stomach Cancer

Gene >> PGR

ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000325455
Start	101049929:101049929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2488A>C
AA Mutation	p.Ile830Leu(p.I830L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128370:101128370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.701G>T
AA Mutation	p.Gly234Val(p.G234V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128194:101128194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Cys(p.R293C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128278:101128278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793G>A
AA Mutation	p.Val265Ile(p.V265I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101062608:101062608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2051T>A
AA Mutation	p.Ile684Asn(p.I684N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101051562:101051562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149186732
CDS Mutation	c.2219G>A
AA Mutation	p.Arg740Gln(p.R740Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101042091:101042091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2500G>A
AA Mutation	p.Gly834Arg(p.G834R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128077:101128077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757746136
CDS Mutation	c.994G>A
AA Mutation	p.Gly332Arg(p.G332R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128815:101128815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.256G>A
AA Mutation	p.Ala86Thr(p.A86T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101051500:101051500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2281T>A
AA Mutation	p.Phe761Ile(p.F761I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101049941:101049941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2476C>G
AA Mutation	p.Leu826Val(p.L826V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128991:101128991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.80T>C
AA Mutation	p.Leu27Pro(p.L27P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128289:101128289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.782C>T
AA Mutation	p.Ala261Val(p.A261V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128290:101128290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781G>C
AA Mutation	p.Ala261Pro(p.A261P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101039185:101039185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2733A>C
AA Mutation	p.Glu911Asp(p.E911D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128677:101128677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.394C>T
AA Mutation	p.Pro132Ser(p.P132S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000325455
Start	101128748:101128748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323G>T
AA Mutation	p.Ser108Ile(p.S108I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101062577:101062577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768803502
CDS Mutation	c.2082T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101128078:101128078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101128669:101128669(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101128384:101128384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101128240:101128240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101128153:101128153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.918G>C
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101128728:101128728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.343T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101128453:101128453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758063171
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101049966:101049966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2451G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325455
Start	101042035:101042035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2556C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000325455
Start	101126159:101126159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1638-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	29
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000325455
Start	101049996:101049998(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2419_2421delGAG
AA Mutation	p.Glu807del(p.E807del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript