Mutation

Primary Site >> Stomach Cancer

Gene >> TRPM4

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49181441:49181441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243C>T
AA Mutation	p.Arg415Trp(p.R415W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49167953:49167953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.304G>A
AA Mutation	p.Val102Ile(p.V102I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49182753:49182753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1439C>T
AA Mutation	p.Ala480Val(p.A480V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49182734:49182734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1420C>T
AA Mutation	p.Arg474Cys(p.R474C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49158212:49158212(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.45C>A
AA Mutation	p.Phe15Leu(p.F15L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49210334:49210334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3257G>A
AA Mutation	p.Arg1086His(p.R1086H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49182711:49182711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1397C>A
AA Mutation	p.Ala466Glu(p.A466E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49168602:49168602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.662T>C
AA Mutation	p.Val221Ala(p.V221A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49210736:49210736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3355C>T
AA Mutation	p.Arg1119Trp(p.R1119W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49189059:49189059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777033881
CDS Mutation	c.1987G>A
AA Mutation	p.Ala663Thr(p.A663T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49168293:49168293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.482G>A
AA Mutation	p.Gly161Asp(p.G161D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000252826
Start	49182801:49182801(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1487C>T
AA Mutation	p.Ala496Val(p.A496V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252826
Start	49182625:49182625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1311G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252826
Start	49183107:49183107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753805994
CDS Mutation	c.1638G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252826
Start	49182802:49182802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1488G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252826
Start	49189013:49189013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779169668
CDS Mutation	c.1941G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000252826
Start	49202127:49202127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746446243
CDS Mutation	c.3117C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252826
Start	49168669:49168669(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.734delG
AA Mutation	p.Gly245AlafsTer33(p.G245Afs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252826
Start	49189018:49189018(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1951delG
AA Mutation	p.Asp651MetfsTer26(p.D651Mfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000252826
Start	49158257:49158257(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.92+1delG
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000252826
Start	49182811:49182812(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1502dupC
AA Mutation	p.Asp502Ter(p.D502*)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	22
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000252826
Start	49200434:49200434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2778+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000252826
Start	49181462:49181462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1263+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript