Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCGCAGGGCTCAGAACTGGCCGGCA[C/T]TGCTCGGGTCGCACTGCAGGAGGCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606722 | ||||||||||||||||||||
Literature Links: |
NCALD 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 |
NCALD - neurocalcin delta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040624.1 | 935 | Missense Mutation | AAT,AGT | N,S 189 | NP_001035714.1 | |
NM_001040625.1 | 935 | Missense Mutation | AAT,AGT | N,S 189 | NP_001035715.1 | |
NM_001040626.1 | 935 | Missense Mutation | AAT,AGT | N,S 189 | NP_001035716.1 | |
NM_001040627.1 | 935 | Missense Mutation | AAT,AGT | N,S 189 | NP_001035717.1 | |
NM_001040628.1 | 935 | Missense Mutation | AAT,AGT | N,S 189 | NP_001035718.1 | |
NM_001040629.1 | 935 | Missense Mutation | AAT,AGT | N,S 189 | NP_001035719.1 | |
NM_001040630.1 | 935 | Missense Mutation | AAT,AGT | N,S 189 | NP_001035720.1 | |
NM_032041.2 | 935 | Missense Mutation | AAT,AGT | N,S 189 | NP_114430.2 | |
XM_011517332.2 | 935 | Missense Mutation | AAT,AGT | N,S 189 | XP_011515634.1 | |
XM_011517333.2 | 935 | Missense Mutation | AAT,AGT | N,S 189 | XP_011515635.1 | |
XM_011517334.2 | 935 | Missense Mutation | AAT,AGT | N,S 189 | XP_011515636.1 | |
XM_011517335.2 | 935 | Missense Mutation | AAT,AGT | N,S 189 | XP_011515637.1 | |
XM_017013900.1 | 935 | Intron | XP_016869389.1 | |||
XM_017013901.1 | 935 | Missense Mutation | AAT,AGT | N,S 189 | XP_016869390.1 | |
XM_017013902.1 | 935 | Missense Mutation | AAT,AGT | N,S 189 | XP_016869391.1 |