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AGAAATTAAGTGGAATAGCAAGTCT[A/G]AAGTCAGGGAAGTCTGTGAGGCCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607955 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SASH1 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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SASH1 - SAM and SH3 domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015278.3 | Intron | NP_056093.3 | ||||
XM_005266875.1 | Intron | XP_005266932.1 | ||||
XM_011535640.1 | Intron | XP_011533942.1 | ||||
XM_017010598.1 | Intron | XP_016866087.1 | ||||
XM_017010599.1 | Intron | XP_016866088.1 | ||||
XM_017010600.1 | Intron | XP_016866089.1 | ||||
XM_017010601.1 | Intron | XP_016866090.1 | ||||
XM_017010602.1 | Intron | XP_016866091.1 | ||||
XM_017010603.1 | Intron | XP_016866092.1 | ||||
XM_017010604.1 | Intron | XP_016866093.1 | ||||
XM_017010605.1 | Intron | XP_016866094.1 | ||||
XM_017010606.1 | Intron | XP_016866095.1 | ||||
XM_017010607.1 | Intron | XP_016866096.1 |