Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGATCACCAATAGCATTCTCTGAGG[C/T]GGAGCTTGATGGAACTTTAATGAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616066 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CCDC169-SOHLH2 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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CCDC169-SOHLH2 - CCDC169-SOHLH2 readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198910.1 | 1561 | Missense Mutation | ACC,GCC | T,A 416 | NP_001185839.1 |
SOHLH2 - spermatogenesis and oogenesis specific basic helix-loop-helix 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001282147.1 | 1561 | Intron | NP_001269076.1 | |||
NM_017826.2 | 1561 | Missense Mutation | ACC,GCC | T,A 339 | NP_060296.2 |
Set Membership: |
HapMap |