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GGAAAAGGAAGAGGCGGCTAAAAAA[C/T]GGCAAGAAGAACAAGAGGTATGGTA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300028 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ZRSR2 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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ZRSR2 - zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005089.3 | 1057 | Intron | NP_005080.1 | |||
XM_005274597.2 | 1057 | UTR 5 | XP_005274654.2 | |||
XM_011545589.2 | 1057 | Missense Mutation | CGG,TGG | R,W 73 | XP_011543891.2 | |
XM_011545590.2 | 1057 | UTR 5 | XP_011543892.2 | |||
XM_017029881.1 | 1057 | Intron | XP_016885370.1 | |||
XM_017029882.1 | 1057 | UTR 5 | XP_016885371.1 | |||
XM_017029883.1 | 1057 | UTR 5 | XP_016885372.1 |