Mutation

Primary Site >> Stomach Cancer

Gene >> HCFC1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153954182:153954182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782239008
CDS Mutation	c.4217C>T
AA Mutation	p.Ala1406Val(p.A1406V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153962297:153962297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782354655
CDS Mutation	c.722C>T
AA Mutation	p.Thr241Met(p.T241M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153960147:153960147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1099C>A
AA Mutation	p.Pro367Thr(p.P367T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153960378:153960378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941T>C
AA Mutation	p.Leu314Pro(p.L314P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153963257:153963257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680G>A
AA Mutation	p.Cys227Tyr(p.C227Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153958210:153958210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1843G>A
AA Mutation	p.Ala615Thr(p.A615T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153954573:153954573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3826G>A
AA Mutation	p.Glu1276Lys(p.E1276K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153958164:153958164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1889G>A
AA Mutation	p.Arg630His(p.R630H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153963423:153963423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514G>T
AA Mutation	p.Asp172Tyr(p.D172Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153950267:153950267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5980G>A
AA Mutation	p.Ala1994Thr(p.A1994T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153955446:153955446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2953C>A
AA Mutation	p.Pro985Thr(p.P985T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153954188:153954188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4211G>A
AA Mutation	p.Gly1404Asp(p.G1404D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153954527:153954527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3872A>G
AA Mutation	p.Asn1291Ser(p.N1291S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153952594:153952594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4862C>A
AA Mutation	p.Ala1621Asp(p.A1621D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153956324:153956324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2723C>T
AA Mutation	p.Thr908Met(p.T908M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153963287:153963287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.650A>G
AA Mutation	p.Lys217Arg(p.K217R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153954215:153954215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4184C>T
AA Mutation	p.Ala1395Val(p.A1395V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153961617:153961617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.829G>A
AA Mutation	p.Val277Ile(p.V277I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000310441
Start	153964247:153964247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183246703
CDS Mutation	c.380C>T
AA Mutation	p.Thr127Met(p.T127M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153954433:153954433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782339413
CDS Mutation	c.3966C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153955072:153955072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782784710
CDS Mutation	c.3327C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153954625:153954625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3774C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153959902:153959902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1344G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153955057:153955057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3342G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153954439:153954439(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782045987
CDS Mutation	c.3960G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153951670:153951670(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377035512
CDS Mutation	c.5298G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	27
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153954463:153954463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375360942
CDS Mutation	c.3936C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	28
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153952716:153952716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201491654
CDS Mutation	c.4740C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	29
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153957372:153957372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782569084
CDS Mutation	c.2295G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	30
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153963229:153963229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.708T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	31
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153959818:153959818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782186278
CDS Mutation	c.1428C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	32
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310441
Start	153954916:153954916(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3483C>A
Mutation Classification	Silent
Feature Type	Transcript

ID	33
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310441
Start	153964237:153964238(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.389dupA
AA Mutation	p.Asn130LysfsTer29(p.N130Kfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript