Mutation

Primary Site >> Stomach Cancer

Gene >> TP73

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3707598:3707598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746207826
CDS Mutation	c.236C>T
AA Mutation	p.Ala79Val(p.A79V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3729424:3729424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530995550
CDS Mutation	c.1172A>G
AA Mutation	p.Gln391Arg(p.Q391R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3733000:3733000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1832A>G
AA Mutation	p.Asp611Gly(p.D611G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378295
Start	3707597:3707597(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781452147
CDS Mutation	c.235G>A
AA Mutation	p.Ala79Thr(p.A79T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3722158:3722158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142165895
CDS Mutation	c.567C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3730057:3730057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139554277
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3722143:3722143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775511685
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378295
Start	3728196:3728196(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752617133
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378295
Start	3728142:3728142(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1004delC
AA Mutation	p.Pro335LeufsTer10(p.P335Lfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000378295
Start	3722204:3722204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.613G>T
AA Mutation	p.Glu205Ter(p.E205*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript