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GCTGTAGCCAAACACTTGAATGTTA[C/T]TGATTTTCATATAGCCCAGGTTCCG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 submissions
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Phenotype: |
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Literature Links: |
BRINP3 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
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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BRINP3 - BMP/retinoic acid inducible neural specific 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317188.1 | 2566 | Missense Mutation | AAT,AGT | N,S 562 | NP_001304117.1 | |
NM_199051.2 | 2566 | Missense Mutation | AAT,AGT | N,S 664 | NP_950252.1 | |
XM_011509472.2 | 2566 | Missense Mutation | AAT,AGT | N,S 634 | XP_011507774.1 | |
XM_011509475.2 | 2566 | Missense Mutation | AAT,AGT | N,S 621 | XP_011507777.1 | |
XM_011509476.2 | 2566 | Missense Mutation | AAT,AGT | N,S 562 | XP_011507778.1 | |
XM_017001125.1 | 2566 | Missense Mutation | AAT,AGT | N,S 664 | XP_016856614.1 | |
XM_017001126.1 | 2566 | Missense Mutation | AAT,AGT | N,S 664 | XP_016856615.1 | |
XM_017001127.1 | 2566 | Missense Mutation | AAT,AGT | N,S 634 | XP_016856616.1 | |
XM_017001128.1 | 2566 | Missense Mutation | AAT,AGT | N,S 634 | XP_016856617.1 | |
XM_017001129.1 | 2566 | Missense Mutation | AAT,AGT | N,S 562 | XP_016856618.1 | |
XM_017001130.1 | 2566 | Missense Mutation | AAT,AGT | N,S 562 | XP_016856619.1 | |
XM_017001131.1 | 2566 | Missense Mutation | AAT,AGT | N,S 371 | XP_016856620.1 | |
XM_017001132.1 | 2566 | Intron | XP_016856621.1 | |||
XM_017001133.1 | 2566 | Intron | XP_016856622.1 |