Primary Site >> Pancreatic Cancer

Gene >> KMT2D

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000301067
Start 49032331:49032331(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12374C>T
AA Mutation p.Ser4125Phe(p.S4125F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000301067
Start 49051114:49051114(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2569A>G
AA Mutation p.Lys857Glu(p.K857E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000301067
Start 49022714:49022714(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs566674356
CDS Mutation c.16214G>A
AA Mutation p.Arg5405His(p.R5405H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000301067
Start 49026311:49026311(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.15655C>A
AA Mutation p.Leu5219Ile(p.L5219I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000301067
Start 49026613:49026613(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.15353C>T
AA Mutation p.Ala5118Val(p.A5118V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000301067
Start 49027090:49027090(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.14876C>T
AA Mutation p.Ala4959Val(p.A4959V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000301067
Start 49031718:49031718(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.12987G>T
AA Mutation p.Gln4329His(p.Q4329H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000301067
Start 49033463:49033463(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.11242C>A
AA Mutation p.Leu3748Ile(p.L3748I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000301067
Start 49041482:49041482(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6288G>T
AA Mutation p.Lys2096Asn(p.K2096N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000301067
Start 49039904:49039904(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773435188
CDS Mutation c.7866C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000301067
Start 49051052:49051052(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2631T>C
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000301067
Start 49033896:49033896(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10809G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000301067
Start 49052134:49052134(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1549delG
AA Mutation p.Glu517SerfsTer413(p.E517Sfs*413)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000301067
Start 49040298:49040299(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.7471dupG
AA Mutation p.Ala2491GlyfsTer15(p.A2491Gfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 15
Mutation Consequence frameshift_variant
Transcription ID ENST00000301067
Start 49039989:49039990(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.7780dupC
AA Mutation p.Leu2594ProfsTer61(p.L2594Pfs*61)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript