Product Details

SNP ID
rs6893639
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:34667114 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTGGTACTGGCTGCTCAGCACTGC[A/G]CTTCTACACATTATACTTTTCTGTT
Phenotype
MIM: 606586
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
LOC105374753 PubMed Links

Gene Details

Gene
LOC105374753
Gene Name
uncharacterized LOC105374753
There are no transcripts associated with this gene.

Gene
RAI14
Gene Name
retinoic acid induced 14
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001145520.1 Intron NP_001138992.1
NM_001145521.1 Intron NP_001138993.1
NM_001145522.1 Intron NP_001138994.1
NM_001145523.1 Intron NP_001138995.1
NM_001145525.1 Intron NP_001138997.1
NM_015577.2 Intron NP_056392.2
XM_006714469.2 Intron XP_006714532.1
XM_011514016.2 Intron XP_011512318.2
XM_011514017.2 Intron XP_011512319.1
XM_011514018.1 Intron XP_011512320.1
XM_011514019.1 Intron XP_011512321.1
XM_011514020.1 Intron XP_011512322.1
XM_011514021.1 Intron XP_011512323.1
XM_011514022.1 Intron XP_011512324.1
XM_011514023.1 Intron XP_011512325.1
XM_011514024.1 Intron XP_011512326.1
XM_011514025.2 Intron XP_011512327.2
XM_017009334.1 Intron XP_016864823.1
XM_017009335.1 Intron XP_016864824.1
XM_017009336.1 Intron XP_016864825.1

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