Product Details

SNP ID
rs114348022
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:8453512 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGTTTCTTCCACGGAAGAAAGTT[A/G]CATCCCAGAATAAAGATCGGCTCTT
Phenotype
MIM: 160994
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HNRNPM PubMed Links

Gene Details

Gene
HNRNPM
Gene Name
heterogeneous nuclear ribonucleoprotein M
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001297418.1 Intron NP_001284347.1
NM_005968.4 Intron NP_005959.2
NM_031203.3 Intron NP_112480.2
XM_005272478.2 Intron XP_005272535.1
XM_005272479.2 Intron XP_005272536.1
XM_005272480.2 Intron XP_005272537.1
XM_005272481.1 Intron XP_005272538.1
XM_005272483.2 Intron XP_005272540.1
XM_017026823.1 Intron XP_016882312.1
XM_017026824.1 Intron XP_016882313.1
XM_017026825.1 Intron XP_016882314.1
XM_017026826.1 Intron XP_016882315.1
XM_017026827.1 Intron XP_016882316.1
XM_017026828.1 Intron XP_016882317.1
XM_017026829.1 Intron XP_016882318.1
XM_017026830.1 Intron XP_016882319.1
XM_017026831.1 Intron XP_016882320.1
XM_017026832.1 Intron XP_016882321.1

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