Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612043 MIM: 612044 MIM: 611954 MIM: 609648 | ||||||||||||||||||||
Literature Links: |
MIR371A PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
MIR371A - microRNA 371a | ||||||
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There are no transcripts associated with this gene. |
MIR371B - microRNA 371b | ||||||
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There are no transcripts associated with this gene. |
MIR372 - microRNA 372 | ||||||
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There are no transcripts associated with this gene. |
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 | 3189 | Missense Mutation | ACC,ATC | T,I 1044 | NP_001264055.1 | |
NM_001277129.1 | 3189 | Missense Mutation | ACC,ATC | T,I 986 | NP_001264058.1 | |
NM_144687.3 | 3189 | Missense Mutation | ACC,ATC | T,I 1043 | NP_653288.1 | |
XM_011527479.1 | 3189 | Missense Mutation | ACC,ATC | T,I 987 | XP_011525781.1 | |
XM_011527480.1 | 3189 | Missense Mutation | ACC,ATC | T,I 987 | XP_011525782.1 | |
XM_011527482.1 | 3189 | Missense Mutation | ACC,ATC | T,I 930 | XP_011525784.1 | |
XM_017027460.1 | 3189 | Missense Mutation | ACC,ATC | T,I 1043 | XP_016882949.1 | |
XM_017027461.1 | 3189 | Missense Mutation | ACC,ATC | T,I 987 | XP_016882950.1 | |
XM_017027462.1 | 3189 | Missense Mutation | ACC,ATC | T,I 986 | XP_016882951.1 | |
XM_017027463.1 | 3189 | Missense Mutation | ACC,ATC | T,I 905 | XP_016882952.1 | |
XM_017027464.1 | 3189 | Missense Mutation | ACC,ATC | T,I 905 | XP_016882953.1 | |
XM_017027465.1 | 3189 | Missense Mutation | ACC,ATC | T,I 905 | XP_016882954.1 | |
XM_017027466.1 | 3189 | Missense Mutation | ACC,ATC | T,I 905 | XP_016882955.1 | |
XM_017027467.1 | 3189 | Missense Mutation | ACC,ATC | T,I 905 | XP_016882956.1 |