Product Details

SNP ID
rs201777064
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:75266746 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAGCCCTGATCTGGAGGCCTAGTC[A/G]GAGACTTCGCTGTAGTAATACTTGT
Phenotype
MIM: 606006 MIM: 612072 MIM: 611974 MIM: 606521
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
GGA3 PubMed Links

Gene Details

Gene
GGA3
Gene Name
golgi associated, gamma adaptin ear containing, ARF binding protein 3
There are no transcripts associated with this gene.

Gene
LOC100287042
Gene Name
uncharacterized LOC100287042
There are no transcripts associated with this gene.

Gene
MIF4GD
Gene Name
MIF4G domain containing
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242498.1 1493 Silent Mutation TCC,TCT S262S NP_001229427.1
NM_001242500.1 1493 Silent Mutation TCC,TCT S255S NP_001229429.1
NM_001242501.1 1493 Silent Mutation TCC,TCT S221S NP_001229430.1
NM_020679.3 1493 Silent Mutation TCC,TCT S255S NP_065730.2
XM_005257530.1 1493 Silent Mutation TCC,TCT S262S XP_005257587.1
XM_005257532.4 1493 Silent Mutation TCC,TCT S221S XP_005257589.1
XM_005257533.1 1493 Silent Mutation TCC,TCT S221S XP_005257590.1
XM_011525051.2 1493 Silent Mutation TCC,TCT S330S XP_011523353.1
XM_011525052.2 1493 Silent Mutation TCC,TCT S323S XP_011523354.1
XM_011525053.2 1493 Silent Mutation TCC,TCT S289S XP_011523355.1
XM_011525054.2 1493 Silent Mutation TCC,TCT S278S XP_011523356.1
XM_011525055.2 1493 Silent Mutation TCC,TCT S237S XP_011523357.1
XM_011525057.2 1493 Silent Mutation TCC,TCT S169S XP_011523359.1
XM_017024888.1 1493 UTR 3 XP_016880377.1
XM_017024889.1 1493 UTR 3 XP_016880378.1
XM_017024890.1 1493 UTR 3 XP_016880379.1
XM_017024891.1 1493 UTR 3 XP_016880380.1
XM_017024892.1 1493 Intron XP_016880381.1
XM_017024893.1 1493 Silent Mutation TCC,TCT S221S XP_016880382.1
XM_017024894.1 1493 Silent Mutation TCC,TCT S221S XP_016880383.1
XM_017024895.1 1493 Silent Mutation TCC,TCT S203S XP_016880384.1
Gene
MRPS7
Gene Name
mitochondrial ribosomal protein S7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_015971.3 1493 Intron NP_057055.2
Gene
SLC25A19
Gene Name
solute carrier family 25 member 19
There are no transcripts associated with this gene.

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