Mutation

Primary Site >> Stomach Cancer

Gene >> TRIM29

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120120609:120120609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1492A>G
AA Mutation	p.Thr498Ala(p.T498A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120127380:120127380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570461440
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Trp(p.R364W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137416:120137416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781322131
CDS Mutation	c.616G>A
AA Mutation	p.Ala206Thr(p.A206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120122995:120122995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768003318
CDS Mutation	c.1394C>T
AA Mutation	p.Pro465Leu(p.P465L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137583:120137583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449G>A
AA Mutation	p.Arg150Gln(p.R150Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120123043:120123043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1346G>A
AA Mutation	p.Arg449His(p.R449H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120125759:120125759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768839001
CDS Mutation	c.1265G>A
AA Mutation	p.Arg422His(p.R422H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137830:120137830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202G>A
AA Mutation	p.Ala68Thr(p.A68T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137961:120137961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.71G>A
AA Mutation	p.Gly24Asp(p.G24D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137455:120137455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.577T>C
AA Mutation	p.Ser193Pro(p.S193P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137713:120137713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765392140
CDS Mutation	c.319G>A
AA Mutation	p.Ala107Thr(p.A107T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000341846
Start	120137596:120137596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436G>A
AA Mutation	p.Gly146Arg(p.G146R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341846
Start	120137810:120137810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.222G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341846
Start	120115395:120115395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1647G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000341846
Start	120137695:120137695(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.337delG
AA Mutation	p.Ala113LeufsTer146(p.A113Lfs*146)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000341846
Start	120137803:120137803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.229C>T
AA Mutation	p.Arg77Ter(p.R77*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript