Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SYMPK

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45827590:45827590(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2101G>T
AA Mutation p.Asp701Tyr(p.D701Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45844069:45844069(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.808T>C
AA Mutation p.Phe270Leu(p.F270L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45848832:45848832(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767015678
CDS Mutation c.344A>G
AA Mutation p.Asn115Ser(p.N115S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45829186:45829186(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1769C>T
AA Mutation p.Ala590Val(p.A590V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45818128:45818128(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2912C>T
AA Mutation p.Ala971Val(p.A971V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45838532:45838532(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs557692962
CDS Mutation c.1171G>A
AA Mutation p.Gly391Ser(p.G391S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45848866:45848866(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.310A>G
AA Mutation p.Ile104Val(p.I104V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45826363:45826363(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2192A>G
AA Mutation p.Gln731Arg(p.Q731R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45822776:45822776(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2771G>A
AA Mutation p.Arg924His(p.R924H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45816957:45816957(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3099G>T
AA Mutation p.Lys1033Asn(p.K1033N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45823445:45823445(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778170949
CDS Mutation c.2627G>A
AA Mutation p.Arg876Gln(p.R876Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45827871:45827871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2033C>T
AA Mutation p.Ala678Val(p.A678V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45854414:45854414(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371089842
CDS Mutation c.82G>A
AA Mutation p.Asp28Asn(p.D28N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000245934
Start 45844045:45844045(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.832T>C
AA Mutation p.Tyr278His(p.Y278H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000245934
Start 45831431:45831431(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs566434106
CDS Mutation c.1551G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000245934
Start 45831419:45831419(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1563G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000245934
Start 45826350:45826350(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2205C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000245934
Start 45829059:45829059(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373014308
CDS Mutation c.1896C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000245934
Start 45815944:45815944(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3594C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000245934
Start 45815890:45815890(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760636520
CDS Mutation c.3648C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000245934
Start 45816037:45816037(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3501delC
AA Mutation p.Ser1168ProfsTer46(p.S1168Pfs*46)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 22
Mutation Consequence frameshift_variant
Transcription ID ENST00000245934
Start 45817999:45817999(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.3041delG
AA Mutation p.Gly1014AlafsTer4(p.G1014Afs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 23
Mutation Consequence stop_gained
Transcription ID ENST00000245934
Start 45847815:45847815(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.613C>T
AA Mutation p.Arg205Ter(p.R205*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence frameshift_variant
Transcription ID ENST00000245934
Start 45835162:45835163(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1308dupC
AA Mutation p.Val437ArgfsTer137(p.V437Rfs*137)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> SYMPK

No Mutation Annotation!