Product Details
- SNP ID
-
rs61732857
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:101689383 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GACGGGTCGCTTTTGGCTCCTCGGA[C/T]GAACTCTTCCAGGGAGAGTTTTCCT
- Phenotype
-
MIM: 606722
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
NCALD
PubMed Links
Gene Details
- Gene
- NCALD
- Gene Name
- neurocalcin delta
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001040624.1 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
NP_001035714.1 |
NM_001040625.1 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
NP_001035715.1 |
NM_001040626.1 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
NP_001035716.1 |
NM_001040627.1 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
NP_001035717.1 |
NM_001040628.1 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
NP_001035718.1 |
NM_001040629.1 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
NP_001035719.1 |
NM_001040630.1 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
NP_001035720.1 |
NM_032041.2 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
NP_114430.2 |
XM_011517332.2 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
XP_011515634.1 |
XM_011517333.2 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
XP_011515635.1 |
XM_011517334.2 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
XP_011515636.1 |
XM_011517335.2 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
XP_011515637.1 |
XM_017013900.1 |
877 |
Intron |
|
|
XP_016869389.1 |
XM_017013901.1 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
XP_016869390.1 |
XM_017013902.1 |
877 |
Missense Mutation |
ATC,GTC |
I170V |
XP_016869391.1 |
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