Mutation

Primary Site >> Stomach Cancer

Gene >> FAM120A

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93557897:93557897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2555G>T
AA Mutation	p.Ser852Ile(p.S852I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93550630:93550630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2213C>G
AA Mutation	p.Ala738Gly(p.A738G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93452240:93452240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325G>A
AA Mutation	p.Val109Ile(p.V109I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93564305:93564305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3122C>A
AA Mutation	p.Ser1041Tyr(p.S1041Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93543249:93543249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1937C>T
AA Mutation	p.Ala646Val(p.A646V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93532242:93532242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1822T>C
AA Mutation	p.Tyr608His(p.Y608H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93557858:93557858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2516G>A
AA Mutation	p.Arg839His(p.R839H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93550612:93550612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2195G>A
AA Mutation	p.Arg732Gln(p.R732Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93564296:93564296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761701846
CDS Mutation	c.3113C>T
AA Mutation	p.Ser1038Leu(p.S1038L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93561187:93561187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2885G>A
AA Mutation	p.Arg962Gln(p.R962Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000277165
Start	93562273:93562273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3014G>A
AA Mutation	p.Gly1005Asp(p.G1005D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93516168:93516168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138093719
CDS Mutation	c.1317G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93498846:93498846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768499030
CDS Mutation	c.990G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93516156:93516156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1305G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93557904:93557904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2562G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93550613:93550613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2196G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93497506:93497506(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745807056
CDS Mutation	c.840C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93452332:93452332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93529448:93529448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1602G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93516186:93516186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1335C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000277165
Start	93557916:93557916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2574G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000277165
Start	93516004:93516004(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1157delG
AA Mutation	p.Gly386AlafsTer27(p.G386Afs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000277165
Start	93498888:93498888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

ID	24
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000277165
Start	93564430:93564447(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3250_3267delGACTCTAAAACGTGCAAT
AA Mutation	p.Asp1084_Asn1089del(p.D1084_N1089del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript