Product Details

SNP ID
rs17489856
Assay Type
Functionally tested
NCBI dbSNP Submissions
19
Location
Chr.1:23306888 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTCTCCAGTCAGTCATCCAATCTAC[C/T]GGTTTCCTCAGAACAACTCCACCCC
Phenotype
MIM: 607201
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HNRNPR PubMed Links

Gene Details

Gene
HNRNPR
Gene Name
heterogeneous nuclear ribonucleoprotein R
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001102397.2 5640 Intron NP_001095867.1
NM_001102398.2 5640 UTR 3 NP_001095868.1
NM_001102399.2 5640 Intron NP_001095869.1
NM_001297620.1 5640 UTR 3 NP_001284549.1
NM_001297621.1 5640 Intron NP_001284550.1
NM_001297622.1 5640 Intron NP_001284551.1
NM_005826.4 5640 UTR 3 NP_005817.1
XM_005245711.4 5640 Intron XP_005245768.1
XM_011540471.2 5640 Intron XP_011538773.1
XM_011540472.2 5640 Intron XP_011538774.1
XM_011540474.2 5640 Intron XP_011538776.1
XM_011540475.2 5640 Intron XP_011538777.1
XM_011540476.2 5640 Intron XP_011538778.1
XM_011540477.2 5640 Intron XP_011538779.1
XM_017000008.1 5640 Intron XP_016855497.1
XM_017000009.1 5640 Intron XP_016855498.1
XM_017000010.1 5640 Intron XP_016855499.1

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