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GTGGCAATTAAAGTTATAGACAAGA[C/T]GGGAGGGCCAGAAGGTGAGCCGGGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 607660 | ||||||||||||||||||||
Literature Links: |
BSDC1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
BSDC1 - BSD domain containing 1 | ||||||
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There are no transcripts associated with this gene. |
FAM229A - family with sequence similarity 229 member A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167676.1 | 572 | Intron | NP_001161148.1 |
TSSK3 - testis specific serine kinase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_052841.3 | 572 | Missense Mutation | ACG,ATG | T,M 44 | NP_443073.1 |