Product Details
- SNP ID
-
rs150358845
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.9:35808591 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CAACGCCATGCACCAGAAATTGCTC[A/G]TATGGCCCTAGCATTACTAGATGCA
- Phenotype
-
MIM: 609997
MIM: 108961
MIM: 605731
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FAM221B
PubMed Links
Gene Details
- Gene
- FAM221B
- Gene Name
- family with sequence similarity 221 member B
There are no transcripts associated with this gene.
- Gene
- HINT2
- Gene Name
- histidine triad nucleotide binding protein 2
There are no transcripts associated with this gene.
- Gene
- NPR2
- Gene Name
- natriuretic peptide receptor 2
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_003995.3 |
6712 |
Missense Mutation |
CAT,CGT |
H932R |
NP_003986.2 |
XM_005251478.3 |
6712 |
Missense Mutation |
CAT,CGT |
H935R |
XP_005251535.1 |
XM_005251479.4 |
6712 |
Missense Mutation |
CAT,CGT |
H606R |
XP_005251536.1 |
XM_011517890.2 |
6712 |
Missense Mutation |
CAT,CGT |
H606R |
XP_011516192.1 |
XM_011517891.2 |
6712 |
Missense Mutation |
CAT,CGT |
H606R |
XP_011516193.1 |
XM_011517892.2 |
6712 |
Missense Mutation |
CAT,CGT |
H606R |
XP_011516194.1 |
XM_011517893.2 |
6712 |
Missense Mutation |
CAT,CGT |
H606R |
XP_011516195.1 |
XM_011517895.2 |
6712 |
Missense Mutation |
CAT,CGT |
H467R |
XP_011516197.1 |
XM_017014745.1 |
6712 |
Missense Mutation |
CAT,CGT |
H606R |
XP_016870234.1 |
XM_017014746.1 |
6712 |
Missense Mutation |
CAT,CGT |
H603R |
XP_016870235.1 |
XM_017014747.1 |
6712 |
Missense Mutation |
CAT,CGT |
H603R |
XP_016870236.1 |
XM_017014748.1 |
6712 |
Missense Mutation |
CAT,CGT |
H464R |
XP_016870237.1 |
XM_017014749.1 |
6712 |
Missense Mutation |
CAT,CGT |
H464R |
XP_016870238.1 |
XM_017014750.1 |
6712 |
Missense Mutation |
CAT,CGT |
H464R |
XP_016870239.1 |
- Gene
- SPAG8
- Gene Name
- sperm associated antigen 8
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