Product Details

SNP ID
rs142148839
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:16409616 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCATTTACATCCCCAAACCCTTAT[A/G]CATTTTATGCAAAAGACATACTGTA
Phenotype
MIM: 608669
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
BNC2 PubMed Links

Gene Details

Gene
BNC2
Gene Name
basonuclin 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001317939.1 17643 UTR 3 NP_001304868.1
NM_001317940.1 17643 UTR 3 NP_001304869.1
NM_017637.5 17643 UTR 3 NP_060107.3
XM_011517924.1 17643 UTR 3 XP_011516226.1
XM_011517934.2 17643 Intron XP_011516236.1
XM_017014816.1 17643 UTR 3 XP_016870305.1
XM_017014817.1 17643 UTR 3 XP_016870306.1
XM_017014818.1 17643 UTR 3 XP_016870307.1
XM_017014819.1 17643 Intron XP_016870308.1
XM_017014820.1 17643 UTR 3 XP_016870309.1
XM_017014821.1 17643 Intron XP_016870310.1
XM_017014822.1 17643 UTR 3 XP_016870311.1
XM_017014823.1 17643 UTR 3 XP_016870312.1
XM_017014824.1 17643 UTR 3 XP_016870313.1
XM_017014825.1 17643 UTR 3 XP_016870314.1
XM_017014826.1 17643 Intron XP_016870315.1
XM_017014827.1 17643 Intron XP_016870316.1
XM_017014828.1 17643 Intron XP_016870317.1
XM_017014829.1 17643 UTR 3 XP_016870318.1

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