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CTGTCCTGAGGTTGGGCCGGGGAGC[A/G]GGTTTGCGGGGTGACAGGAGGGTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600566 MIM: 607096 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NRXN2 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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NRXN2 - neurexin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015080.3 | 2956 | Silent Mutation | CCC,CCT | P,P 1532 | NP_055895.1 | |
NM_138732.2 | 2956 | Silent Mutation | CCC,CCT | P,P 1462 | NP_620060.1 | |
NM_138734.2 | 2956 | Silent Mutation | CCC,CCT | P,P 486 | NP_620063.1 | |
XM_005274400.3 | 2956 | Silent Mutation | CCC,CCT | P,P 1525 | XP_005274457.1 | |
XM_005274401.3 | 2956 | Intron | XP_005274458.1 | |||
XM_005274402.3 | 2956 | Intron | XP_005274459.1 | |||
XM_011545370.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1535 | XP_011543672.1 | |
XM_011545371.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1534 | XP_011543673.1 | |
XM_011545373.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1528 | XP_011543675.1 | |
XM_011545375.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1520 | XP_011543677.1 | |
XM_011545385.1 | 2956 | Silent Mutation | CCC,CCT | P,P 797 | XP_011543687.1 | |
XM_017018563.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1525 | XP_016874052.1 | |
XM_017018564.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1524 | XP_016874053.1 | |
XM_017018565.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1523 | XP_016874054.1 | |
XM_017018566.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1511 | XP_016874055.1 | |
XM_017018567.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1505 | XP_016874056.1 | |
XM_017018568.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1502 | XP_016874057.1 | |
XM_017018569.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1501 | XP_016874058.1 | |
XM_017018570.1 | 2956 | Intron | XP_016874059.1 | |||
XM_017018571.1 | 2956 | Intron | XP_016874060.1 | |||
XM_017018572.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1300 | XP_016874061.1 | |
XM_017018573.1 | 2956 | Intron | XP_016874062.1 | |||
XM_017018574.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1290 | XP_016874063.1 | |
XM_017018575.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1289 | XP_016874064.1 | |
XM_017018576.1 | 2956 | Silent Mutation | CCC,CCT | P,P 1116 | XP_016874065.1 | |
XM_017018577.1 | 2956 | Silent Mutation | CCC,CCT | P,P 794 | XP_016874066.1 | |
XM_017018578.1 | 2956 | Intron | XP_016874067.1 |
SLC22A12 - solute carrier family 22 member 12 | ||||||
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There are no transcripts associated with this gene. |