Mutation

Primary Site >> Stomach Cancer

Gene >> CDK12

ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39517535:39517535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2942G>A
AA Mutation	p.Arg981His(p.R981H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39515738:39515738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2776C>A
AA Mutation	p.Leu926Ile(p.L926I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000447079
Start	39511630:39511630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2768G>T
AA Mutation	p.Gly923Val(p.G923V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39494610:39494610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2335C>T
AA Mutation	p.Arg779Cys(p.R779C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39494611:39494611(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2336G>A
AA Mutation	p.Arg779His(p.R779H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39509740:39509740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2645G>A
AA Mutation	p.Arg882Gln(p.R882Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39511605:39511605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2743C>T
AA Mutation	p.Pro915Ser(p.P915S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39470958:39470958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1126A>G
AA Mutation	p.Ser376Gly(p.S376G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39524850:39524850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3272C>T
AA Mutation	p.Pro1091Leu(p.P1091L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39525906:39525906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3350C>A
AA Mutation	p.Ala1117Glu(p.A1117E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39462432:39462432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361G>C
AA Mutation	p.Asp121His(p.D121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39470964:39470964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370304179
CDS Mutation	c.1132C>T
AA Mutation	p.Arg378Cys(p.R378C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000447079
Start	39525906:39525906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3350C>T
AA Mutation	p.Ala1117Val(p.A1117V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447079
Start	39492859:39492859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2217C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447079
Start	39530707:39530707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780009851
CDS Mutation	c.3864C>T
Mutation Classification	Silent
Feature Type	Transcript

ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447079
Start	39471188:39471188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1356A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447079
Start	39494585:39494585(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2310A>G
Mutation Classification	Silent
Feature Type	Transcript

ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000447079
Start	39530648:39530648(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3810delC
AA Mutation	p.Gly1271AspfsTer23(p.G1271Dfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000447079
Start	39490669:39490669(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2048delC
AA Mutation	p.Pro683GlnfsTer70(p.P683Qfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000447079
Start	39471639:39471639(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1811delC
AA Mutation	p.Pro604LeufsTer6(p.P604Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000447079
Start	39531179:39531179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4336G>T
AA Mutation	p.Gly1446Ter(p.G1446*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	22
Mutation Consequence	stop_gained
Transcription ID	ENST00000447079
Start	39530909:39530909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4066C>T
AA Mutation	p.Arg1356Ter(p.R1356*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000447079
Start	39462898:39462899(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.828dupT
AA Mutation	p.Pro277SerfsTer21(p.P277Sfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript