Mutation

Primary Site >> Stomach Cancer

Gene >> TBC1D9

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140657799:140657799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1935C>A
AA Mutation	p.Asp645Glu(p.D645E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140634065:140634065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2629C>A
AA Mutation	p.Leu877Ile(p.L877I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140669705:140669705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766891520
CDS Mutation	c.1366G>A
AA Mutation	p.Val456Ile(p.V456I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140668994:140668994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764603749
CDS Mutation	c.1511G>A
AA Mutation	p.Arg504His(p.R504H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140662098:140662098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766985680
CDS Mutation	c.1598A>G
AA Mutation	p.Asn533Ser(p.N533S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140669663:140669663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763242846
CDS Mutation	c.1408C>T
AA Mutation	p.Arg470Trp(p.R470W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140677066:140677066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.887G>A
AA Mutation	p.Arg296His(p.R296H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140624361:140624361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2927A>G
AA Mutation	p.Gln976Arg(p.Q976R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140669732:140669732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781475633
CDS Mutation	c.1339C>T
AA Mutation	p.Arg447Cys(p.R447C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000442267
Start	140679078:140679078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715A>G
AA Mutation	p.Asn239Asp(p.N239D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140686443:140686443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.261C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140677023:140677023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140662025:140662025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748711159
CDS Mutation	c.1671G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140669640:140669640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749048911
CDS Mutation	c.1431G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000442267
Start	140622567:140622567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3429C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442267
Start	140670910:140670910(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1076delA
AA Mutation	p.Lys359ArgfsTer20(p.K359Rfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442267
Start	140679689:140679689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.515delA
AA Mutation	p.Lys172ArgfsTer33(p.K172Rfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000442267
Start	140678959:140678959(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.834delA
AA Mutation	p.Val279CysfsTer4(p.V279Cfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	stop_gained
Transcription ID	ENST00000442267
Start	140670863:140670863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1123C>T
AA Mutation	p.Arg375Ter(p.R375*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	20
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000442267
Start	140677072:140677077(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.876_881delTGAGAG
AA Mutation	p.Ser292_Glu293del(p.S292_E293del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript