Primary Site >> Stomach Cancer

Gene >> ULK2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361658
Start 19816763:19816763(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1082C>T
AA Mutation p.Ser361Leu(p.S361L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361658
Start 19801894:19801894(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1324A>G
AA Mutation p.Ser442Gly(p.S442G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361658
Start 19783791:19783791(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2366G>A
AA Mutation p.Ser789Asn(p.S789N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361658
Start 19781926:19781926(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2602G>A
AA Mutation p.Val868Met(p.V868M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000361658
Start 19786083:19786083(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2105C>T
AA Mutation p.Pro702Leu(p.P702L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000361658
Start 19801836:19801836(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1382A>G
AA Mutation p.Gln461Arg(p.Q461R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000361658
Start 19786047:19786047(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2141C>T
AA Mutation p.Ala714Val(p.A714V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000361658
Start 19816849:19816849(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.996A>G
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000361658
Start 19781905:19781905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2623C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000361658
Start 19845313:19845313(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770928670
CDS Mutation c.534G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000361658
Start 19843130:19843130(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.636A>G
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000361658
Start 19783760:19783760(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2397C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000361658
Start 19826140:19826140(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.834delA
AA Mutation p.Lys278AsnfsTer130(p.K278Nfs*130)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000361658
Start 19826176:19826176(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.798delT
AA Mutation p.Phe266LeufsTer11(p.F266Lfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000361658
Start 19841506:19841507(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.686dupA
AA Mutation p.Asn229LysfsTer7(p.N229Kfs*7)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript