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GAAGCTGGAGGCTGGGTACTTGAGC[C/T]GACACAGTAGGTGAAGGAGAGGCTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 164005 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NFIX PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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NFIX - nuclear factor I X | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | 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 |