Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MLLT10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21612418:21612418(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.476A>C
AA Mutation p.Lys159Thr(p.K159T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21673600:21673600(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1302A>C
AA Mutation p.Glu434Asp(p.E434D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21595420:21595420(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.385C>T
AA Mutation p.Pro129Ser(p.P129S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21713897:21713897(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1825G>A
AA Mutation p.Ala609Thr(p.A609T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21595339:21595339(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.304C>G
AA Mutation p.His102Asp(p.H102D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21670453:21670453(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.800A>G
AA Mutation p.Tyr267Cys(p.Y267C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21733943:21733943(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2672C>T
AA Mutation p.Ala891Val(p.A891V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21735174:21735174(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374332871
CDS Mutation c.2894G>A
AA Mutation p.Arg965Gln(p.R965Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21595354:21595354(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.319C>A
AA Mutation p.Leu107Met(p.L107M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000307729
Start 21670544:21670544(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.891C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000307729
Start 21673523:21673523(version: GRCh38)
Mutation Type DEL
dbSNP_RS rs774092366
CDS Mutation c.1231delG
AA Mutation p.Val411Ter(p.V411*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000307729
Start 21740105:21740105(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3031delC
AA Mutation p.Leu1011CysfsTer11(p.L1011Cfs*11)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000307729
Start 21740107:21740107(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3033delG
AA Mutation p.Gln1012ArgfsTer10(p.Q1012Rfs*10)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000307729
Start 21612429:21612429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.487C>T
AA Mutation p.Arg163Ter(p.R163*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000307729
Start 21673706:21673706(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1408G>T
AA Mutation p.Gly470Ter(p.G470*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000307729
Start 21731023:21731024(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.2192dupT
AA Mutation p.Leu731PhefsTer8(p.L731Ffs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> MLLT10

Mutation ID 1
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000307729
Start 21727928:21727928(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2063G>T
AA Mutation p.Arg688Leu(p.R688L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21586334:21586334(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.281G>T
AA Mutation p.Arg94Ile(p.R94I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21595382:21595382(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.347A>G
AA Mutation p.Asn116Ser(p.N116S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21670503:21670503(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.850G>A
AA Mutation p.Asp284Asn(p.D284N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000307729
Start 21673433:21673433(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1135G>A
AA Mutation p.Asp379Asn(p.D379N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000307729
Start 21741940:21741940(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3164G>T
AA Mutation p.Arg1055Ile(p.R1055I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000307729
Start 21740089:21740089(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3015A>G
Mutation Classification Silent
Feature Type Transcript