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TGAGAGCGCCTTTCTGCCCACCTGC[A/T]CCCAGGGGGCCCTTCTGTCCTGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610982 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
INF2 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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INF2 - inverted formin, FH2 and WH2 domain containing | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031714.3 | Intron | NP_001026884.3 | ||||
NM_022489.3 | Intron | NP_071934.3 | ||||
NM_032714.2 | Intron | NP_116103.1 | ||||
XM_005268004.4 | Intron | XP_005268061.1 | ||||
XM_005268005.4 | Intron | XP_005268062.1 | ||||
XM_017021595.1 | Intron | XP_016877084.1 |