Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TRPM6

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74775981:74775981(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3305C>A
AA Mutation p.Pro1102His(p.P1102H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74858686:74858686(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.96C>G
AA Mutation p.Ser32Arg(p.S32R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74785991:74785991(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2802T>A
AA Mutation p.Phe934Leu(p.F934L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74812389:74812389(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1353T>A
AA Mutation p.Asp451Glu(p.D451E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74821790:74821790(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.889C>T
AA Mutation p.Pro297Ser(p.P297S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74785983:74785983(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs558534348
CDS Mutation c.2810C>T
AA Mutation p.Ala937Val(p.A937V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74776007:74776007(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3279G>T
AA Mutation p.Met1093Ile(p.M1093I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74762027:74762027(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4644G>T
AA Mutation p.Glu1548Asp(p.E1548D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74762949:74762949(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3722G>T
AA Mutation p.Arg1241Ile(p.R1241I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74840212:74840212(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.356A>C
AA Mutation p.Lys119Thr(p.K119T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74821777:74821777(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.902T>C
AA Mutation p.Leu301Pro(p.L301P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74801977:74801977(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1930C>A
AA Mutation p.Leu644Ile(p.L644I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74739768:74739768(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5442G>T
AA Mutation p.Trp1814Cys(p.W1814C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74738437:74738437(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs146677759
CDS Mutation c.5746C>T
AA Mutation p.Arg1916Trp(p.R1916W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74812339:74812339(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373324464
CDS Mutation c.1403G>A
AA Mutation p.Arg468His(p.R468H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74821778:74821778(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.901C>A
AA Mutation p.Leu301Met(p.L301M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74775961:74775961(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3325A>C
AA Mutation p.Ser1109Arg(p.S1109R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74775892:74775892(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751099197
CDS Mutation c.3394G>A
AA Mutation p.Val1132Ile(p.V1132I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74796751:74796751(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2381G>A
AA Mutation p.Ser794Asn(p.S794N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74728322:74728322(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143161006
CDS Mutation c.5852C>T
AA Mutation p.Pro1951Leu(p.P1951L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74744128:74744128(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5101A>C
AA Mutation p.Lys1701Gln(p.K1701Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74755367:74755367(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4892A>C
AA Mutation p.Lys1631Thr(p.K1631T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74820419:74820419(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147157434
CDS Mutation c.1019G>A
AA Mutation p.Arg340Gln(p.R340Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74750711:74750711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5010A>C
AA Mutation p.Lys1670Asn(p.K1670N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74808140:74808140(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1532T>C
AA Mutation p.Ile511Thr(p.I511T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74842321:74842321(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.175G>A
AA Mutation p.Gly59Arg(p.G59R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74739433:74739433(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5504G>T
AA Mutation p.Arg1835Ile(p.R1835I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74796820:74796820(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2312T>C
AA Mutation p.Val771Ala(p.V771A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74802078:74802078(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1829A>G
AA Mutation p.Asp610Gly(p.D610G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74739854:74739854(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142946646
CDS Mutation c.5356G>A
AA Mutation p.Val1786Ile(p.V1786I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74775939:74775939(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3347G>T
AA Mutation p.Arg1116Leu(p.R1116L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74782407:74782407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3164T>A
AA Mutation p.Phe1055Tyr(p.F1055Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence synonymous_variant
Transcription ID ENST00000360774
Start 74887833:74887833(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.24G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 34
Mutation Consequence synonymous_variant
Transcription ID ENST00000360774
Start 74816708:74816708(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770756456
CDS Mutation c.1269T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 35
Mutation Consequence synonymous_variant
Transcription ID ENST00000360774
Start 74739378:74739378(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5559C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 36
Mutation Consequence synonymous_variant
Transcription ID ENST00000360774
Start 74762519:74762519(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4152T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 37
Mutation Consequence synonymous_variant
Transcription ID ENST00000360774
Start 74762054:74762054(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4617T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 38
Mutation Consequence synonymous_variant
Transcription ID ENST00000360774
Start 74887830:74887830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.27C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 39
Mutation Consequence synonymous_variant
Transcription ID ENST00000360774
Start 74775983:74775983(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3303G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 40
Mutation Consequence synonymous_variant
Transcription ID ENST00000360774
Start 74762786:74762786(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3885G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 41
Mutation Consequence frameshift_variant
Transcription ID ENST00000360774
Start 74728308:74728308(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.5866delG
AA Mutation p.Glu1956LysfsTer25(p.E1956Kfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 42
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000360774
Start 74785876:74785876(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.2917delA
AA Mutation p.Met973Ter(p.M973*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 43
Mutation Consequence stop_gained
Transcription ID ENST00000360774
Start 74724681:74724681(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6001G>T
AA Mutation p.Glu2001Ter(p.E2001*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence stop_gained
Transcription ID ENST00000360774
Start 74762287:74762287(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4384G>T
AA Mutation p.Glu1462Ter(p.E1462*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence stop_gained
Transcription ID ENST00000360774
Start 74820420:74820420(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750008274
CDS Mutation c.1018C>T
AA Mutation p.Arg340Ter(p.R340*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> TRPM6

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74762027:74762027(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4644G>T
AA Mutation p.Glu1548Asp(p.E1548D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74803878:74803878(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1647A>C
AA Mutation p.Arg549Ser(p.R549S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74816903:74816903(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1196C>T
AA Mutation p.Ala399Val(p.A399V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74788703:74788703(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2578G>A
AA Mutation p.Val860Met(p.V860M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74821808:74821808(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.871C>A
AA Mutation p.Leu291Met(p.L291M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74782789:74782789(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2984G>A
AA Mutation p.Arg995His(p.R995H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74816957:74816957(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1142T>G
AA Mutation p.Ile381Arg(p.I381R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74724737:74724737(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5945G>T
AA Mutation p.Arg1982Ile(p.R1982I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74782739:74782739(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3034G>T
AA Mutation p.Asp1012Tyr(p.D1012Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000360774
Start 74747907:74747907(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5065A>C
AA Mutation p.Ser1689Arg(p.S1689R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000360774
Start 74762614:74762614(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4057C>T
AA Mutation p.Arg1353Ter(p.R1353*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript