Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AACCATGGGTTATTGCAGTGGCAGG[G/T]GCACGCTTATCTTTATCTGTGGCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609758 | ||||||||||||||||||||
Literature Links: |
NKAIN2 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 |
NKAIN2 - Na+/K+ transporting ATPase interacting 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040214.2 | 381 | Missense Mutation | GGC,TGC | G,C 8 | NP_001035304.1 | |
NM_001300737.1 | 381 | UTR 5 | NP_001287666.1 | |||
NM_001300738.1 | 381 | UTR 5 | NP_001287667.1 | |||
NM_001300740.1 | 381 | Intron | NP_001287669.1 | |||
NM_153355.4 | 381 | Missense Mutation | GGC,TGC | G,C 8 | NP_699186.2 | |
XM_011535501.2 | 381 | Missense Mutation | GGC,TGC | G,C 8 | XP_011533803.1 | |
XM_011535502.2 | 381 | Intron | XP_011533804.1 | |||
XM_011535503.2 | 381 | Missense Mutation | GGC,TGC | G,C 8 | XP_011533805.1 | |
XM_017010318.1 | 381 | Missense Mutation | GGC,TGC | G,C 8 | XP_016865807.1 | |
XM_017010319.1 | 381 | Missense Mutation | GGC,TGC | G,C 8 | XP_016865808.1 |