Primary Site >> Stomach Cancer

Gene >> MYO1C

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000359786
Start 1480597:1480597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.836A>G
AA Mutation p.Asn279Ser(p.N279S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000359786
Start 1474666:1474666(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1741A>T
AA Mutation p.Ile581Phe(p.I581F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000359786
Start 1468048:1468048(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147835827
CDS Mutation c.2836G>A
AA Mutation p.Ala946Thr(p.A946T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000359786
Start 1470662:1470662(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2240G>T
AA Mutation p.Gly747Val(p.G747V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000359786
Start 1471962:1471962(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs758453580
CDS Mutation c.1966C>T
AA Mutation p.Arg656Cys(p.R656C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000359786
Start 1484195:1484195(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760702315
CDS Mutation c.184G>A
AA Mutation p.Ala62Thr(p.A62T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359786
Start 1477505:1477505(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769630282
CDS Mutation c.1574C>T
AA Mutation p.Thr525Met(p.T525M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000359786
Start 1478088:1478088(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778512232
CDS Mutation c.1400C>T
AA Mutation p.Ala467Val(p.A467V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000359786
Start 1480610:1480610(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.823G>C
AA Mutation p.Val275Leu(p.V275L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000359786
Start 1474834:1474834(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1694T>C
AA Mutation p.Leu565Pro(p.L565P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000359786
Start 1470196:1470196(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs139792172
CDS Mutation c.2505G>A
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000359786
Start 1467284:1467284(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370307852
CDS Mutation c.3123G>A
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000359786
Start 1482981:1482981(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201404300
CDS Mutation c.426C>T
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000359786
Start 1483639:1483639(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.318C>T
Mutation Classification Silent
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000359786
Start 1467863:1467863(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2944C>T
AA Mutation p.Gln982Ter(p.Q982*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence stop_gained
Transcription ID ENST00000359786
Start 1492478:1492478(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.10C>T
AA Mutation p.Gln4Ter(p.Q4*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000359786
Start 1471122:1471123(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.2160dupC
AA Mutation p.Lys721GlnfsTer122(p.K721Qfs*122)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript