Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTGCCTAGCCCACCCGGCTCCCCGA[G/T]GACCCAGGAAAGCTGCGGCATTGCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610702 | ||||||||||||||||||||
Literature Links: |
HSPA12B 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 |
HSPA12B - heat shock protein family A (Hsp70) member 12B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001197327.1 | 234 | Missense Mutation | AGG,ATG | R,M 31 | NP_001184256.1 | |
NM_001318322.1 | 234 | Intron | NP_001305251.1 | |||
NM_052970.4 | 234 | Missense Mutation | AGG,ATG | R,M 31 | NP_443202.3 | |
XM_011529151.2 | 234 | Intron | XP_011527453.1 | |||
XM_017027632.1 | 234 | Missense Mutation | AGG,ATG | R,M 31 | XP_016883121.1 | |
XM_017027633.1 | 234 | Missense Mutation | AGG,ATG | R,M 31 | XP_016883122.1 | |
XM_017027634.1 | 234 | Missense Mutation | AGG,ATG | R,M 31 | XP_016883123.1 | |
XM_017027635.1 | 234 | Missense Mutation | AGG,ATG | R,M 31 | XP_016883124.1 |