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TTCACTCACCTGGAGGTTTGGTTCG[C/T]GGAAGTGAATCATGTCACAGAAGTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
WSCD2 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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WSCD2 - WSC domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001304447.1 | Intron | NP_001291376.1 | ||||
NM_014653.3 | Intron | NP_055468.2 | ||||
XM_017020243.1 | Intron | XP_016875732.1 | ||||
XM_017020244.1 | Intron | XP_016875733.1 | ||||
XM_017020245.1 | Intron | XP_016875734.1 | ||||
XM_017020246.1 | Intron | XP_016875735.1 | ||||
XM_017020247.1 | Intron | XP_016875736.1 | ||||
XM_017020248.1 | Intron | XP_016875737.1 | ||||
XM_017020249.1 | Intron | XP_016875738.1 | ||||
XM_017020250.1 | Intron | XP_016875739.1 | ||||
XM_017020251.1 | Intron | XP_016875740.1 | ||||
XM_017020252.1 | Intron | XP_016875741.1 |