Product Details

SNP ID
rs59576871
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:49641209 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGAAGCATAGAGCCTGGCCTGTGGA[C/G]ATGTTTTTAGTATTGGTGGGGAGCT
Phenotype
MIM: 616288
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FMNL3 PubMed Links

Gene Details

Gene
FMNL3
Gene Name
formin like 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_175736.4 8018 UTR 3 NP_783863.4
NM_198900.2 8018 UTR 3 NP_944489.2
XM_005269218.2 8018 UTR 3 XP_005269275.1
XM_011538968.2 8018 UTR 3 XP_011537270.1
XM_011538969.2 8018 UTR 3 XP_011537271.1
XM_011538970.2 8018 UTR 3 XP_011537272.1
XM_011538971.2 8018 UTR 3 XP_011537273.1
XM_011538972.2 8018 UTR 3 XP_011537274.1
XM_011538973.2 8018 UTR 3 XP_011537275.2
XM_011538974.2 8018 UTR 3 XP_011537276.1
Gene
PRPF40B
Gene Name
pre-mRNA processing factor 40 homolog B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001031698.2 8018 Intron NP_001026868.2
NM_012272.2 8018 Intron NP_036404.1
XM_006719324.3 8018 Intron XP_006719387.1
XM_006719325.3 8018 Intron XP_006719388.1
XM_011538135.2 8018 Intron XP_011536437.1
XM_011538136.2 8018 Intron XP_011536438.1
XM_011538137.2 8018 Intron XP_011536439.1
XM_011538138.2 8018 Intron XP_011536440.1
XM_011538139.2 8018 Intron XP_011536441.1
XM_011538140.2 8018 Intron XP_011536442.1
XM_011538141.1 8018 Intron XP_011536443.1
XM_011538143.2 8018 Intron XP_011536445.1
XM_011538144.2 8018 Intron XP_011536446.1
XM_017019135.1 8018 Intron XP_016874624.1
XM_017019136.1 8018 Intron XP_016874625.1
XM_017019137.1 8018 Intron XP_016874626.1
XM_017019138.1 8018 Intron XP_016874627.1
XM_017019139.1 8018 Intron XP_016874628.1

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