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- SNP ID:
- rs34542615
- Gene
-
NGF - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 115286119 - 115286119 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GCTGAGCACACACACACAGGCCGTA[C/T]CTATCCGGATAAACCGCCAGGCAGC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 162030
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Literature Links: |
NGF 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 |
| NGF - nerve growth factor | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_002506.2 | 846 | Missense Mutation | GAT,GGT | D,G 226 | NP_002497.2 | |
| XM_006710663.3 | 846 | Missense Mutation | GAT,GGT | D,G 226 | XP_006710726.1 | |
| XM_011541518.2 | 846 | Missense Mutation | GAT,GGT | D,G 281 | XP_011539820.1 | |
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