Mutation

Primary Site >> Stomach Cancer

Gene >> MS4A14

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60416421:60416421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376488191
CDS Mutation	c.1453C>T
AA Mutation	p.Arg485Trp(p.R485W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60416217:60416217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1249C>T
AA Mutation	p.Pro417Ser(p.P417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60415917:60415917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949C>A
AA Mutation	p.Pro317Thr(p.P317T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60416980:60416980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2012T>G
AA Mutation	p.Leu671Arg(p.L671R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60416905:60416905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1937C>A
AA Mutation	p.Ser646Tyr(p.S646Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60415706:60415706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738A>C
AA Mutation	p.Glu246Asp(p.E246D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60415603:60415603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.635T>C
AA Mutation	p.Leu212Pro(p.L212P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60400419:60400419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780301996
CDS Mutation	c.283T>C
AA Mutation	p.Tyr95His(p.Y95H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60402925:60402925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146613208
CDS Mutation	c.332C>T
AA Mutation	p.Thr111Met(p.T111M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60415744:60415744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776C>A
AA Mutation	p.Pro259His(p.P259H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60400434:60400434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768900672
CDS Mutation	c.298G>A
AA Mutation	p.Asp100Asn(p.D100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000300187
Start	60416149:60416149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1181C>A
AA Mutation	p.Ala394Asp(p.A394D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300187
Start	60416540:60416540(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300187
Start	60415874:60415874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.906A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300187
Start	60415556:60415556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.588T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300187
Start	60415808:60415808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.840A>G
Mutation Classification	Silent
Feature Type	Transcript