Mutation

Primary Site >> Stomach Cancer

Gene >> INHBA

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41689864:41689864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1067G>A
AA Mutation	p.Ser356Asn(p.S356N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41700290:41700290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85C>T
AA Mutation	p.His29Tyr(p.H29Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690177:41690177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754G>A
AA Mutation	p.Ala252Thr(p.A252T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41700251:41700251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690005:41690005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.926G>A
AA Mutation	p.Arg309Gln(p.R309Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690293:41690293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638C>T
AA Mutation	p.Ala213Val(p.A213V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41700154:41700154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.221T>C
AA Mutation	p.Val74Ala(p.V74A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690291:41690291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.640C>T
AA Mutation	p.Arg214Trp(p.R214W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690446:41690446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485C>A
AA Mutation	p.Pro162His(p.P162H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41700130:41700130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245C>T
AA Mutation	p.Ala82Val(p.A82V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41689795:41689795(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1136G>A
AA Mutation	p.Arg379Gln(p.R379Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41689681:41689681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1250A>G
AA Mutation	p.Asn417Ser(p.N417S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000242208
Start	41690003:41690003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.928C>T
AA Mutation	p.Arg310Trp(p.R310W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242208
Start	41690214:41690214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370035610
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242208
Start	41690067:41690067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864G>A
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000242208
Start	41689821:41689821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1110A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242208
Start	41690129:41690129(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.802delG
AA Mutation	p.Glu268LysfsTer91(p.E268Kfs*91)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242208
Start	41690451:41690451(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.480delA
AA Mutation	p.Val161SerfsTer37(p.V161Sfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript