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CCAAACGTGACCACTGCCACCCCGT[C/T]ACTCCCCGATGCTCACCACAGTTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611954 MIM: 609648 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR373 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MIR373 - microRNA 373 | ||||||
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There are no transcripts associated with this gene. |
NLRP12 - NLR family pyrin domain containing 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277126.1 | Intron | NP_001264055.1 | ||||
NM_001277129.1 | Intron | NP_001264058.1 | ||||
NM_144687.3 | Intron | NP_653288.1 | ||||
XM_011527479.1 | Intron | XP_011525781.1 | ||||
XM_011527480.1 | Intron | XP_011525782.1 | ||||
XM_011527482.1 | Intron | XP_011525784.1 | ||||
XM_017027460.1 | Intron | XP_016882949.1 | ||||
XM_017027461.1 | Intron | XP_016882950.1 | ||||
XM_017027462.1 | Intron | XP_016882951.1 | ||||
XM_017027463.1 | Intron | XP_016882952.1 | ||||
XM_017027464.1 | Intron | XP_016882953.1 | ||||
XM_017027465.1 | Intron | XP_016882954.1 | ||||
XM_017027466.1 | Intron | XP_016882955.1 | ||||
XM_017027467.1 | Intron | XP_016882956.1 |