Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGTTTTAGATCCTTCACAGCTGTA[A/C]CTACTGAAAGTACATTTTTATTGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601448 | ||||||||||||||||||||
Literature Links: |
NPAT 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 |
NPAT - nuclear protein, coactivator of histone transcription | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321307.1 | 4538 | Missense Mutation | GGT,GTT | G,V 1231 | NP_001308236.1 | |
NM_002519.2 | 4538 | Missense Mutation | GGT,GTT | G,V 1224 | NP_002510.2 | |
XM_011542854.2 | 4538 | Missense Mutation | GGT,GTT | G,V 1233 | XP_011541156.1 | |
XM_017017802.1 | 4538 | Missense Mutation | GGT,GTT | G,V 1165 | XP_016873291.1 | |
XM_017017803.1 | 4538 | Missense Mutation | GGT,GTT | G,V 1165 | XP_016873292.1 |