Product Details

SNP ID
rs10072272
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.5:145590389 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TAGCATTTATTACAATCTAACATTT[C/T]CTTATTATTTATGTATGTGTTTGCT
Phenotype
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PRELID2 PubMed Links

Gene Details

Gene
PRELID2
Gene Name
PRELI domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_138492.5 Intron NP_612501.3
NM_182960.3 Intron NP_892005.1
NM_205846.2 Intron NP_995318.1
XM_017009127.1 Intron XP_016864616.1
XM_017009128.1 Intron XP_016864617.1
XM_017009129.1 Intron XP_016864618.1
XM_017009130.1 Intron XP_016864619.1
XM_017009131.1 Intron XP_016864620.1
XM_017009132.1 Intron XP_016864621.1
XM_017009133.1 Intron XP_016864622.1
XM_017009134.1 Intron XP_016864623.1
XM_017009135.1 Intron XP_016864624.1

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