Mutation

Primary Site >> Stomach Cancer

Gene >> PIWIL1

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000245255
Start	130349252:130349252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.748C>T
AA Mutation	p.Pro250Ser(p.P250S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000245255
Start	130371515:130371515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745487305
CDS Mutation	c.2503G>T
AA Mutation	p.Ala835Ser(p.A835S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000245255
Start	130361564:130361564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753282833
CDS Mutation	c.1933G>A
AA Mutation	p.Ala645Thr(p.A645T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000245255
Start	130349942:130349942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1019T>C
AA Mutation	p.Val340Ala(p.V340A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000245255
Start	130361213:130361213(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1699A>G
AA Mutation	p.Lys567Glu(p.K567E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245255
Start	130355556:130355556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138596008
CDS Mutation	c.1293C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245255
Start	130371224:130371224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2370T>G
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245255
Start	130349404:130349404(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900C>G
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245255
Start	130371574:130371574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2562G>T
Mutation Classification	Silent
Feature Type	Transcript

ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245255
Start	130361269:130361269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1755T>C
Mutation Classification	Silent
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245255
Start	130346512:130346512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766051497
CDS Mutation	c.459C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000245255
Start	130357523:130357523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1635A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000245255
Start	130356926:130356926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1413C>A
AA Mutation	p.Tyr471Ter(p.Y471*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000245255
Start	130371182:130371183(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.2334dupT
AA Mutation	p.Ile779TyrfsTer10(p.I779Yfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript