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AATAGATGGGCACACCCTTTAACTT[A/G]ATATCGACCAGTAAAGCCTGCAGTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607379 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NF2 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
|
NF2 - neurofibromin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000268.3 | Intron | NP_000259.1 | ||||
NM_016418.5 | Intron | NP_057502.2 | ||||
NM_181825.2 | Intron | NP_861546.1 | ||||
NM_181828.2 | Intron | NP_861966.1 | ||||
NM_181829.2 | Intron | NP_861967.1 | ||||
NM_181830.2 | Intron | NP_861968.1 | ||||
NM_181831.2 | Intron | NP_861969.1 | ||||
NM_181832.2 | Intron | NP_861970.1 | ||||
NM_181833.2 | Intron | NP_861971.1 | ||||
XM_017028809.1 | Intron | XP_016884298.1 | ||||
XM_017028810.1 | Intron | XP_016884299.1 |