Mutation

Primary Site >> Stomach Cancer

Gene >> CDAN1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42731675:42731675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1684C>A
AA Mutation	p.Pro562Thr(p.P562T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42729077:42729077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2591G>T
AA Mutation	p.Arg864Leu(p.R864L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42729092:42729092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370476233
CDS Mutation	c.2576C>T
AA Mutation	p.Pro859Leu(p.P859L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42733988:42733988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1317T>A
AA Mutation	p.Asn439Lys(p.N439K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42736061:42736061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587G>T
AA Mutation	p.Arg196Met(p.R196M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42730632:42730632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs80338696
CDS Mutation	c.2140C>T
AA Mutation	p.Arg714Trp(p.R714W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42736031:42736031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772703075
CDS Mutation	c.617G>A
AA Mutation	p.Arg206Gln(p.R206Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356231
Start	42734254:42734254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373881679
CDS Mutation	c.1229G>A
AA Mutation	p.Arg410Gln(p.R410Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42729337:42729337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766040108
CDS Mutation	c.2433G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42727672:42727672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758732191
CDS Mutation	c.3045C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42726155:42726155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3210G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42725230:42725230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3472C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42730753:42730753(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780807045
CDS Mutation	c.2019C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356231
Start	42731784:42731784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756319452
CDS Mutation	c.1575C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356231
Start	42731673:42731673(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1686delC
AA Mutation	p.Thr563ProfsTer29(p.T563Pfs*29)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356231
Start	42727692:42727692(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3025delG
AA Mutation	p.Glu1009SerfsTer23(p.E1009Sfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000356231
Start	42728221:42728221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2851G>T
AA Mutation	p.Glu951Ter(p.E951*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000356231
Start	42733164:42733164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1390C>T
AA Mutation	p.Arg464Ter(p.R464*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript