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ATGATCTGCTCAGGGTTGTAGCTCC[A/G]TATGCCACCCAGGCGCCACCTGCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609632 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GDPD5 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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GDPD5 - glycerophosphodiester phosphodiesterase domain containing 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030792.6 | 2845 | Missense Mutation | CGG,TGG | R,W 526 | NP_110419.5 | |
XM_006718697.3 | 2845 | Missense Mutation | CGG,TGG | R,W 526 | XP_006718760.1 | |
XM_011545276.2 | 2845 | Missense Mutation | CGG,TGG | R,W 526 | XP_011543578.1 | |
XM_011545277.2 | 2845 | Missense Mutation | CGG,TGG | R,W 526 | XP_011543579.1 | |
XM_011545278.2 | 2845 | Missense Mutation | CGG,TGG | R,W 526 | XP_011543580.1 | |
XM_011545279.2 | 2845 | Missense Mutation | CGG,TGG | R,W 526 | XP_011543581.1 | |
XM_011545280.1 | 2845 | Missense Mutation | CGG,TGG | R,W 469 | XP_011543582.1 | |
XM_011545281.2 | 2845 | Missense Mutation | CGG,TGG | R,W 388 | XP_011543583.1 | |
XM_011545285.2 | 2845 | Missense Mutation | CGG,TGG | R,W 388 | XP_011543587.1 | |
XM_011545286.1 | 2845 | Missense Mutation | CGG,TGG | R,W 281 | XP_011543588.1 | |
XM_011545287.1 | 2845 | Missense Mutation | CGG,TGG | R,W 281 | XP_011543589.1 |
KLHL35 - kelch like family member 35 | ||||||
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There are no transcripts associated with this gene. |