Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
GAB4 PubMed Links | |||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese)
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EUR - Not Available | |||||
AMR - Not Available |
GAB4 - GRB2 associated binding protein family member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001037814.1 | 978 | Missense Mutation | AAC,AGC | N,S 526 | NP_001032903.1 | |
XM_011546114.2 | 978 | Missense Mutation | AAC,AGC | N,S 374 | XP_011544416.1 | |
XM_011546115.1 | 978 | Missense Mutation | AAC,AGC | N,S 303 | XP_011544417.1 | |
XM_011546116.2 | 978 | Intron | XP_011544418.1 | |||
XM_011546117.1 | 978 | Missense Mutation | AAC,AGC | N,S 285 | XP_011544419.1 | |
XM_017028575.1 | 978 | Missense Mutation | AAC,AGC | N,S 527 | XP_016884064.1 | |
XM_017028576.1 | 978 | Missense Mutation | AAC,AGC | N,S 294 | XP_016884065.1 |
Set Membership: |
HapMap |