Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611686 MIM: 604149 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
CASD1 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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Japanese
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JPT (Japanese)
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AFR
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Chinese
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CHB (Han Chinese)
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EUR
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AMR
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CASD1 - CAS1 domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022900.4 | Intron | NP_075051.4 | ||||
XM_006716092.3 | Intron | XP_006716155.1 | ||||
XM_006716093.3 | Intron | XP_006716156.2 | ||||
XM_011516495.2 | Intron | XP_011514797.1 | ||||
XM_017012546.1 | Intron | XP_016868035.1 | ||||
XM_017012547.1 | Intron | XP_016868036.1 |
SGCE - sarcoglycan epsilon | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001099400.1 | Intron | NP_001092870.1 | ||||
NM_001099401.1 | Intron | NP_001092871.1 | ||||
NM_001301139.1 | Intron | NP_001288068.1 | ||||
NM_003919.2 | Intron | NP_003910.1 | ||||
XM_005250675.4 | Intron | XP_005250732.1 | ||||
XM_005250677.4 | Intron | XP_005250734.1 | ||||
XM_011516663.2 | Intron | XP_011514965.1 | ||||
XM_011516664.2 | Intron | XP_011514966.1 | ||||
XM_011516665.2 | Intron | XP_011514967.1 | ||||
XM_011516666.2 | Intron | XP_011514968.1 | ||||
XM_011516667.2 | Intron | XP_011514969.1 | ||||
XM_011516669.2 | Intron | XP_011514971.1 | ||||
XM_017012763.1 | Intron | XP_016868252.1 | ||||
XM_017012764.1 | Intron | XP_016868253.1 | ||||
XM_017012765.1 | Intron | XP_016868254.1 | ||||
XM_017012766.1 | Intron | XP_016868255.1 | ||||
XM_017012767.1 | Intron | XP_016868256.1 | ||||
XM_017012768.1 | Intron | XP_016868257.1 | ||||
XM_017012769.1 | Intron | XP_016868258.1 | ||||
XM_017012770.1 | Intron | XP_016868259.1 |
Set Membership: |
HapMap Validated |