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AACTGAGCTCTATGGGACAGGAGCA[A/G]TGGATTTTGGAGTAGGTGGCTTTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612275 MIM: 610275 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GGNBP2 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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GGNBP2 - gametogenetin binding protein 2 | ||||||
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There are no transcripts associated with this gene. |
MYO19 - myosin XIX | ||||||
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There are no transcripts associated with this gene. |
PIGW - phosphatidylinositol glycan anchor biosynthesis class W | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_178517.3 | 798 | Missense Mutation | ATG,GTG | M,V 167 | NP_848612.2 | |
XM_005257238.2 | 798 | Missense Mutation | ATG,GTG | M,V 167 | XP_005257295.1 | |
XM_011524646.2 | 798 | Missense Mutation | ATG,GTG | M,V 167 | XP_011522948.1 |