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SNP ID:
rs1045079
Gene
HNRNPR
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.1: 23309601 - 23309601 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

GAACACCAATCAATGAAAGTGCTAA[C/T]TGGAATAAATACTTGAATTTAGACT

Assay ID C___7474151_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 31 submissions

Phenotype:

 MIM: 607201

Literature Links:

 HNRNPR PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.07)
(0.93)
Caucasian
C (0.00)
(1.00)
CEPH (CEU) - Not Available
EAS
G (0.00)
(1.00)
African American
C (0.20)
(0.80)
YRI (Yoruba)
G (0.28)
(0.72)
SAS
G (0.00)
(1.00)
Chinese - Not Available CHB (Han Chinese) - Not Available
AFR
G (0.26)
(0.74)
Japanese - Not Available JPT (Japanese) - Not Available
EUR
G (0.00)
(1.00)
AMR
G (0.03)
(0.97)
HNRNPR - heterogeneous nuclear ribonucleoprotein R
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_001102397.2 2927 Intron NP_001095867.1
NM_001102398.2 2927 UTR 3 NP_001095868.1
NM_001102399.2 2927 Intron NP_001095869.1
NM_001297620.1 2927 UTR 3 NP_001284549.1
NM_001297621.1 2927 Intron NP_001284550.1
NM_001297622.1 2927 Intron NP_001284551.1
NM_005826.4 2927 UTR 3 NP_005817.1
XM_005245711.4 2927 Intron XP_005245768.1
XM_011540471.2 2927 Intron XP_011538773.1
XM_011540472.2 2927 Intron XP_011538774.1
XM_011540474.2 2927 Intron XP_011538776.1
XM_011540475.2 2927 Intron XP_011538777.1
XM_011540476.2 2927 Intron XP_011538778.1
XM_011540477.2 2927 Intron XP_011538779.1
XM_017000008.1 2927 Intron XP_016855497.1
XM_017000009.1 2927 Intron XP_016855498.1
XM_017000010.1 2927 Intron XP_016855499.1

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