Product Details

SNP ID
rs145138372
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:89729235 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAAGCCTCATTGTCAGGATCCACAG[G/T]CATATCTTCCAGAATTCCTTCCTGT
Phenotype
MIM: 163890
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
SNCA PubMed Links

Gene Details

Gene
SNCA
Gene Name
synuclein alpha
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000345.3 419 Missense Mutation NP_000336.1
NM_001146054.1 419 Missense Mutation NP_001139526.1
NM_001146055.1 419 Missense Mutation NP_001139527.1
NM_007308.2 419 Intron NP_009292.1
XM_011532203.1 419 Intron XP_011530505.1
XM_011532204.2 419 Intron XP_011530506.1
XM_011532205.2 419 Intron XP_011530507.1
XM_011532206.1 419 Intron XP_011530508.1
XM_011532207.1 419 Intron XP_011530509.1
XM_011532208.2 419 Missense Mutation XP_011530510.1
XM_017008562.1 419 Missense Mutation XP_016864051.1
XM_017008563.1 419 Missense Mutation XP_016864052.1

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