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ATGTTTTTTCCATTCAAGTATACAT[G/T]TAATTCGACATGGTCATAAGTAATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607866 | ||||||||||||||||||||
Literature Links: |
SPRYD7 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 |
SPRYD7 - SPRY domain containing 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127482.2 | 684 | Missense Mutation | AAT,CAT | N,H 101 | NP_001120954.1 | |
NM_020456.3 | 684 | Missense Mutation | AAT,CAT | N,H 140 | NP_065189.1 | |
XM_017020677.1 | 684 | Missense Mutation | AAT,CAT | N,H 140 | XP_016876166.1 |