Mutation

Primary Site >> Stomach Cancer

Gene >> RB1CC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000025008
Start	52683670:52683670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248G>A
AA Mutation	p.Arg83His(p.R83H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000025008
Start	52660611:52660611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1674G>T
AA Mutation	p.Trp558Cys(p.W558C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000025008
Start	52660612:52660612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1673G>C
AA Mutation	p.Trp558Ser(p.W558S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000025008
Start	52636058:52636058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775020996
CDS Mutation	c.4349A>G
AA Mutation	p.His1450Arg(p.H1450R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000025008
Start	52657716:52657716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2113A>G
AA Mutation	p.Ile705Val(p.I705V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000025008
Start	52656635:52656635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3194C>T
AA Mutation	p.Ala1065Val(p.A1065V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000025008
Start	52660979:52660979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1574A>C
AA Mutation	p.Lys525Thr(p.K525T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000025008
Start	52656767:52656767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3062A>C
AA Mutation	p.Asn1021Thr(p.N1021T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000025008
Start	52661214:52661214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746797101
CDS Mutation	c.1426G>A
AA Mutation	p.Val476Ile(p.V476I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000025008
Start	52661582:52661582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1311T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000025008
Start	52656610:52656610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3219A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000025008
Start	52661191:52661191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1449C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000025008
Start	52683639:52683639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374755456
CDS Mutation	c.279G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000025008
Start	52657393:52657393(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2436A>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000025008
Start	52628072:52628072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4596A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000025008
Start	52656214:52656214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771579613
CDS Mutation	c.3615C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000025008
Start	52656317:52656317(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3512delA
AA Mutation	p.Asn1171ThrfsTer2(p.N1171Tfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000025008
Start	52656175:52656175(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3654delA
AA Mutation	p.Lys1218AsnfsTer13(p.K1218Nfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000025008
Start	52657279:52657279(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs772155322
CDS Mutation	c.2550delA
AA Mutation	p.Val851Ter(p.V851*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000025008
Start	52656938:52656938(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2891delA
AA Mutation	p.Lys964SerfsTer13(p.K964Sfs*13)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000025008
Start	52657147:52657147(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2682delA
AA Mutation	p.Lys894AsnfsTer2(p.K894Nfs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000025008
Start	52660644:52660645(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1640dupT
AA Mutation	p.Leu547PhefsTer7(p.L547Ffs*7)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	23
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000025008
Start	52657996:52657996(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1920+2C>G
Mutation Classification	Splice_Site
Feature Type	Transcript