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- SNP ID:
- rs377056909
- Gene
-
BNC2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.9: 16437210 - 16437210 on Build GRCh38
- Polymorphism:
- T/C, Transition substitution
- Context Sequence [VIC/FAM]:
CTAGCAGTGGTGCTGAGACAGGGTT[T/C]ATGTACTGGAATGGAAGCAGAAATG
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608669
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Literature Links: |
BNC2 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 |
| BNC2 - basonuclin 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001317939.1 | 5813 | Missense Mutation | ATA,ATG | I,M 286 | NP_001304868.1 | |
| NM_001317940.1 | 5813 | Missense Mutation | ATA,ATG | I,M 233 | NP_001304869.1 | |
| NM_017637.5 | 5813 | Missense Mutation | ATA,ATG | I,M 328 | NP_060107.3 | |
| XM_011517924.1 | 5813 | Missense Mutation | ATA,ATG | I,M 286 | XP_011516226.1 | |
| XM_011517934.2 | 5813 | Missense Mutation | ATA,ATG | I,M 154 | XP_011516236.1 | |
| XM_017014816.1 | 5813 | Missense Mutation | ATA,ATG | I,M 370 | XP_016870305.1 | |
| XM_017014817.1 | 5813 | Missense Mutation | ATA,ATG | I,M 370 | XP_016870306.1 | |
| XM_017014818.1 | 5813 | Missense Mutation | ATA,ATG | I,M 342 | XP_016870307.1 | |
| XM_017014819.1 | 5813 | Missense Mutation | ATA,ATG | I,M 370 | XP_016870308.1 | |
| XM_017014820.1 | 5813 | Missense Mutation | ATA,ATG | I,M 370 | XP_016870309.1 | |
| XM_017014821.1 | 5813 | Missense Mutation | ATA,ATG | I,M 342 | XP_016870310.1 | |
| XM_017014822.1 | 5813 | Missense Mutation | ATA,ATG | I,M 219 | XP_016870311.1 | |
| XM_017014823.1 | 5813 | Missense Mutation | ATA,ATG | I,M 219 | XP_016870312.1 | |
| XM_017014824.1 | 5813 | Missense Mutation | ATA,ATG | I,M 154 | XP_016870313.1 | |
| XM_017014825.1 | 5813 | Missense Mutation | ATA,ATG | I,M 370 | XP_016870314.1 | |
| XM_017014826.1 | 5813 | Missense Mutation | ATA,ATG | I,M 370 | XP_016870315.1 | |
| XM_017014827.1 | 5813 | Missense Mutation | ATA,ATG | I,M 370 | XP_016870316.1 | |
| XM_017014828.1 | 5813 | Missense Mutation | ATA,ATG | I,M 370 | XP_016870317.1 | |
| XM_017014829.1 | 5813 | Missense Mutation | ATA,ATG | I,M 93 | XP_016870318.1 | |
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