Mutation

Primary Site >> Stomach Cancer

Gene >> PYGM

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64754794:64754794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757387408
CDS Mutation	c.898G>A
AA Mutation	p.Val300Met(p.V300M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64758281:64758281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493G>T
AA Mutation	p.Gly165Trp(p.G165W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64759855:64759855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44G>A
AA Mutation	p.Ser15Asn(p.S15N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64755530:64755530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.689C>A
AA Mutation	p.Pro230His(p.P230H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64759778:64759778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764465584
CDS Mutation	c.121G>A
AA Mutation	p.Val41Ile(p.V41I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64753135:64753135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1456G>A
AA Mutation	p.Gly486Ser(p.G486S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64755296:64755296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762779955
CDS Mutation	c.832C>T
AA Mutation	p.Arg278Cys(p.R278C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64753642:64753642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756303162
CDS Mutation	c.1280G>A
AA Mutation	p.Arg427Gln(p.R427Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64751424:64751424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143217651
CDS Mutation	c.1870G>A
AA Mutation	p.Val624Ile(p.V624I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64759717:64759717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145514333
CDS Mutation	c.182G>A
AA Mutation	p.Arg61His(p.R61H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000164139
Start	64755491:64755491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728G>A
AA Mutation	p.Arg243His(p.R243H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000164139
Start	64753572:64753572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000164139
Start	64758459:64758459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372262267
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000164139
Start	64758273:64758273(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.501delT
AA Mutation	p.Phe167LeufsTer128(p.F167Lfs*128)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000164139
Start	64747228:64747232(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2304_2308delCCATG
AA Mutation	p.His768GlnfsTer4(p.H768Qfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000164139
Start	64752000:64752004(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1688_1692delTCTTC
AA Mutation	p.Leu563ArgfsTer11(p.L563Rfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000164139
Start	64753125:64753125(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1466delC
AA Mutation	p.Pro489LeufsTer50(p.P489Lfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000164139
Start	64751626:64751627(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1797dupT
AA Mutation	p.Val600CysfsTer35(p.V600Cfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000164139
Start	64759858:64759859(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.40dupA
AA Mutation	p.Ile14AsnfsTer14(p.I14Nfs*14)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript