Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RASGRP2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64728973:64728973(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1661G>A
AA Mutation p.Ser554Asn(p.S554N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64739369:64739369(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.804G>T
AA Mutation p.Glu268Asp(p.E268D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64740969:64740969(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs781543360
CDS Mutation c.350G>A
AA Mutation p.Ser117Asn(p.S117N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64729791:64729791(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1562G>A
AA Mutation p.Gly521Asp(p.G521D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64740970:64740970(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.349A>T
AA Mutation p.Ser117Cys(p.S117C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000354024
Start 64740949:64740949(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375059620
CDS Mutation c.370G>A
AA Mutation p.Val124Ile(p.V124I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64739725:64739725(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776573272
CDS Mutation c.607G>A
AA Mutation p.Val203Ile(p.V203I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64730115:64730115(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1492G>A
AA Mutation p.Val498Ile(p.V498I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64730126:64730126(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1481G>A
AA Mutation p.Arg494His(p.R494H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64736976:64736976(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.872G>A
AA Mutation p.Arg291His(p.R291H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64735180:64735180(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1344G>T
AA Mutation p.Gln448His(p.Q448H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64742097:64742097(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.89T>C
AA Mutation p.Val30Ala(p.V30A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64736865:64736865(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs771246989
CDS Mutation c.983G>A
AA Mutation p.Arg328Gln(p.R328Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000354024
Start 64736954:64736954(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.894C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000354024
Start 64740977:64740977(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.342G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000354024
Start 64742105:64742105(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.81C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000354024
Start 64730128:64730128(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1479delG
AA Mutation p.Arg494AlafsTer25(p.R494Afs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 18
Mutation Consequence frameshift_variant
Transcription ID ENST00000354024
Start 64742054:64742054(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.132delC
AA Mutation p.Trp45GlyfsTer29(p.W45Gfs*29)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 19
Mutation Consequence stop_lost
Transcription ID ENST00000354024
Start 64727302:64727302(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1830A>T
AA Mutation p.Ter610TyrextTer1(p.*610Yext*1)
Mutation Classification Nonstop_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> RASGRP2

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000354024
Start 64735175:64735175(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1349A>C
AA Mutation p.Glu450Ala(p.E450A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000354024
Start 64740962:64740962(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.357C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 3
Mutation Consequence splice_donor_variant
Transcription ID ENST00000354024
Start 64739358:64739358(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.813+2T>A
Mutation Classification Splice_Site
Feature Type Transcript