Product Details

SNP ID
rs55892736
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:12998646 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCAAGAAACAGAGACACAACCAGG[A/G]TGTGAACTCACGTACACCACCATCA
Phenotype
MIM: 164005
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NFIX PubMed Links

Gene Details

Gene
NFIX
Gene Name
nuclear factor I X
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001271043.2 Intron NP_001257972.1
NM_001271044.2 Intron NP_001257973.1
NM_002501.3 Intron NP_002492.2
XM_005259917.4 Intron XP_005259974.1
XM_005259918.4 Intron XP_005259975.1
XM_005259919.3 Intron XP_005259976.1
XM_005259920.3 Intron XP_005259977.1
XM_006722760.2 Intron XP_006722823.1
XM_011528040.1 Intron XP_011526342.1
XM_017026837.1 Intron XP_016882326.1

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