Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGAGATTACATTGAAAGAGTCTCT[C/T]GCCTGTGTGTGATCTCTTGTGGATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
ZSCAN5A 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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ZSCAN5A - zinc finger and SCAN domain containing 5A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001322061.1 | 1490 | Missense Mutation | AAG,GAG | K,E 433 | NP_001308990.1 | |
NM_001322062.1 | 1490 | Intron | NP_001308991.1 | |||
NM_001322064.1 | 1490 | Missense Mutation | AAG,GAG | K,E 381 | NP_001308993.1 | |
NM_001322065.1 | 1490 | Missense Mutation | AAG,GAG | K,E 381 | NP_001308994.1 | |
NM_001322066.1 | 1490 | Missense Mutation | AAG,GAG | K,E 381 | NP_001308995.1 | |
NM_001322067.1 | 1490 | Missense Mutation | AAG,GAG | K,E 381 | NP_001308996.1 | |
NM_001322068.1 | 1490 | Missense Mutation | AAG,GAG | K,E 381 | NP_001308997.1 | |
NM_001322069.1 | 1490 | Missense Mutation | AAG,GAG | K,E 381 | NP_001308998.1 | |
NM_001322070.1 | 1490 | Missense Mutation | AAG,GAG | K,E 381 | NP_001308999.1 | |
NM_001322072.1 | 1490 | Missense Mutation | AAG,GAG | K,E 381 | NP_001309001.1 | |
NM_001322073.1 | 1490 | Missense Mutation | AAG,GAG | K,E 380 | NP_001309002.1 | |
NM_001322074.1 | 1490 | Missense Mutation | AAG,GAG | K,E 380 | NP_001309003.1 | |
NM_001322075.1 | 1490 | Missense Mutation | AAG,GAG | K,E 380 | NP_001309004.1 | |
NM_001322076.1 | 1490 | Missense Mutation | AAG,GAG | K,E 380 | NP_001309005.1 | |
NM_001322077.1 | 1490 | Missense Mutation | AAG,GAG | K,E 264 | NP_001309006.1 | |
NM_001322078.1 | 1490 | Missense Mutation | AAG,GAG | K,E 251 | NP_001309007.1 | |
NM_024303.2 | 1490 | Intron | NP_077279.1 | |||
XM_005259254.1 | 1490 | Intron | XP_005259311.1 | |||
XM_006723377.3 | 1490 | Missense Mutation | AAG,GAG | K,E 456 | XP_006723440.1 | |
XM_011527308.1 | 1490 | Intron | XP_011525610.1 | |||
XM_017027298.1 | 1490 | Missense Mutation | AAG,GAG | K,E 457 | XP_016882787.1 | |
XM_017027299.1 | 1490 | Missense Mutation | AAG,GAG | K,E 380 | XP_016882788.1 |