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CTGTTGACTCTGAAAGGCAAGGAAC[C/T]CCTGTGTGGCGGAGATGGTGGCCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608121 MIM: 608122 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PARVB 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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PARVB - parvin beta | ||||||
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There are no transcripts associated with this gene. |
PARVG - parvin gamma | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001137605.2 | Intron | NP_001131077.1 | ||||
NM_022141.6 | Intron | NP_071424.1 | ||||
XM_005261702.3 | Intron | XP_005261759.1 | ||||
XM_011530302.2 | Intron | XP_011528604.1 | ||||
XM_017028907.1 | Intron | XP_016884396.1 | ||||
XM_017028908.1 | Intron | XP_016884397.1 |