Mutation

Primary Site >> Stomach Cancer

Gene >> SPECC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20232264:20232264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2210A>T
AA Mutation	p.Asp737Val(p.D737V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20246066:20246066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765903879
CDS Mutation	c.2492G>A
AA Mutation	p.Arg831His(p.R831H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20096655:20096655(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763091276
CDS Mutation	c.4C>T
AA Mutation	p.Arg2Trp(p.R2W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20110536:20110536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764238558
CDS Mutation	c.257C>T
AA Mutation	p.Thr86Met(p.T86M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20204978:20204978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.929G>A
AA Mutation	p.Arg310Gln(p.R310Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20232242:20232242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2188A>T
AA Mutation	p.Thr730Ser(p.T730S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20205195:20205195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1146A>C
AA Mutation	p.Glu382Asp(p.E382D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20096718:20096718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765479679
CDS Mutation	c.67C>T
AA Mutation	p.Arg23Trp(p.R23W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20232317:20232317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2263G>C
AA Mutation	p.Glu755Gln(p.E755Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20232318:20232318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2264A>T
AA Mutation	p.Glu755Val(p.E755V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20314061:20314061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530436980
CDS Mutation	c.3203C>T
AA Mutation	p.Thr1068Met(p.T1068M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000261503
Start	20205770:20205770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761861967
CDS Mutation	c.1721C>T
AA Mutation	p.Thr574Met(p.T574M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261503
Start	20205207:20205207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1158C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261503
Start	20205810:20205810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1761C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261503
Start	20110543:20110543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.264C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261503
Start	20205357:20205357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1308A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261503
Start	20246022:20246022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs533160344
CDS Mutation	c.2448G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000261503
Start	20205423:20205423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1374T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261503
Start	20204950:20204950(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.908delA
AA Mutation	p.Asn303ThrfsTer63(p.N303Tfs*63)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261503
Start	20232355:20232355(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2305delG
AA Mutation	p.Asp769MetfsTer81(p.D769Mfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000261503
Start	20096675:20096675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24G>A
AA Mutation	p.Trp8Ter(p.W8*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261503
Start	20096752:20096753(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.103dupT
AA Mutation	p.Ser35PhefsTer2(p.S35Ffs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript