Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> A2M

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9095000:9095000(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2098C>G
AA Mutation p.Pro700Ala(p.P700A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9109968:9109968(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.572C>A
AA Mutation p.Ser191Tyr(p.S191Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9110019:9110019(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs369574498
CDS Mutation c.521G>A
AA Mutation p.Arg174His(p.R174H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9076761:9076761(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3527A>T
AA Mutation p.Lys1176Met(p.K1176M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9072690:9072690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3938G>A
AA Mutation p.Ser1313Asn(p.S1313N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9099416:9099416(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1666G>A
AA Mutation p.Ala556Thr(p.A556T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9090373:9090373(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2579T>C
AA Mutation p.Val860Ala(p.V860A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9110014:9110014(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774076635
CDS Mutation c.526G>A
AA Mutation p.Ala176Thr(p.A176T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9090419:9090419(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2533C>T
AA Mutation p.Pro845Ser(p.P845S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9109393:9109393(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763515018
CDS Mutation c.686T>C
AA Mutation p.Phe229Ser(p.F229S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9069806:9069806(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4202G>T
AA Mutation p.Arg1401Ile(p.R1401I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9072398:9072398(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4064C>A
AA Mutation p.Pro1355His(p.P1355H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9091274:9091274(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2396C>T
AA Mutation p.Pro799Leu(p.P799L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9093546:9093546(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2159T>C
AA Mutation p.Leu720Pro(p.L720P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9079277:9079277(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3086G>T
AA Mutation p.Gly1029Val(p.G1029V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9110020:9110020(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756179835
CDS Mutation c.520C>T
AA Mutation p.Arg174Cys(p.R174C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9090000:9090000(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373992205
CDS Mutation c.2620G>A
AA Mutation p.Ala874Thr(p.A874T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9093510:9093510(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2195G>A
AA Mutation p.Arg732Gln(p.R732Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9099467:9099467(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs780559648
CDS Mutation c.1615C>T
AA Mutation p.Arg539Trp(p.R539W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9070496:9070496(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4186G>A
AA Mutation p.Val1396Met(p.V1396M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9079665:9079665(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3005C>A
AA Mutation p.Ser1002Tyr(p.S1002Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9101585:9101585(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1356C>A
AA Mutation p.Phe452Leu(p.F452L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9077787:9077787(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3190A>G
AA Mutation p.Thr1064Ala(p.T1064A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9074596:9074596(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3720G>T
AA Mutation p.Lys1240Asn(p.K1240N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9106260:9106260(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1080A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9107581:9107581(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs202126909
CDS Mutation c.822C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9106588:9106588(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.897C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9091231:9091231(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375292452
CDS Mutation c.2439G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9098712:9098712(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs754296966
CDS Mutation c.1746C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9109880:9109880(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.660C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 31
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9090001:9090001(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767057851
CDS Mutation c.2619C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 32
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9107563:9107563(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.840T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 33
Mutation Consequence stop_gained
Transcription ID ENST00000318602
Start 9077770:9077770(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3207G>A
AA Mutation p.Trp1069Ter(p.W1069*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence stop_gained
Transcription ID ENST00000318602
Start 9079750:9079750(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2920G>T
AA Mutation p.Glu974Ter(p.E974*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence splice_donor_variant
Transcription ID ENST00000318602
Start 9077344:9077344(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3351+2T>C
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> A2M

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9068823:9068823(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4283G>A
AA Mutation p.Ser1428Asn(p.S1428N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9091356:9091356(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2314C>A
AA Mutation p.Leu772Met(p.L772M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9112458:9112458(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773505902
CDS Mutation c.349C>T
AA Mutation p.Arg117Trp(p.R117W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9077757:9077757(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3220C>A
AA Mutation p.Gln1074Lys(p.Q1074K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000318602
Start 9098608:9098608(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs531579697
CDS Mutation c.1850C>T
AA Mutation p.Ser617Leu(p.S617L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9079765:9079765(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769823302
CDS Mutation c.2905C>T
AA Mutation p.Pro969Ser(p.P969S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000318602
Start 9070496:9070496(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4186G>A
AA Mutation p.Val1396Met(p.V1396M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9113384:9113384(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752368777
CDS Mutation c.246C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000318602
Start 9077758:9077758(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3219G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000318602
Start 9090434:9090434(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2518G>T
AA Mutation p.Glu840Ter(p.E840*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript