Product Details

SNP ID
rs16921055
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:20782056 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TAATGTTTATATAGCTCAACTCTAT[A/G]TAAATCCACAAAGAACCTTTCAGAA
Phenotype
MIM: 605491
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NEBL PubMed Links

Gene Details

Gene
NEBL
Gene Name
nebulette
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001173484.1 7129 UTR 3 NP_001166955.1
NM_006393.2 7129 UTR 3 NP_006384.1
NM_213569.2 7129 UTR 3 NP_998734.1
XM_005252342.4 7129 UTR 3 XP_005252399.1
XM_005252343.4 7129 UTR 3 XP_005252400.1
XM_005252344.4 7129 UTR 3 XP_005252401.1
XM_011519291.2 7129 UTR 3 XP_011517593.1
XM_017015467.1 7129 UTR 3 XP_016870956.1
XM_017015468.1 7129 UTR 3 XP_016870957.1
XM_017015469.1 7129 Intron XP_016870958.1

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