Product Details
- SNP ID
-
rs185330742
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
6
- Location
-
Chr.1:16399437 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGGTCTAGTGCATAGTGGTTGCTC[A/G]GCTGCCTACGGACCATCTTCTTGTC
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SPATA21
PubMed Links
Gene Details
- Gene
- SPATA21
- Gene Name
- spermatogenesis associated 21
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_198546.1 |
2254 |
Missense Mutation |
CCG,CTG |
P420L |
NP_940948.1 |
| XM_011541407.2 |
2254 |
Missense Mutation |
CCG,CTG |
P646L |
XP_011539709.1 |
| XM_011541417.2 |
2254 |
Intron |
|
|
XP_011539719.1 |
| XM_017001216.1 |
2254 |
Missense Mutation |
CCG,CTG |
P646L |
XP_016856705.1 |
| XM_017001217.1 |
2254 |
Missense Mutation |
CCG,CTG |
P602L |
XP_016856706.1 |
| XM_017001218.1 |
2254 |
Intron |
|
|
XP_016856707.1 |
| XM_017001219.1 |
2254 |
Intron |
|
|
XP_016856708.1 |
| XM_017001220.1 |
2254 |
Missense Mutation |
CCG,CTG |
P470L |
XP_016856709.1 |
| XM_017001221.1 |
2254 |
Missense Mutation |
CCG,CTG |
P397L |
XP_016856710.1 |
| XM_017001222.1 |
2254 |
Missense Mutation |
CCG,CTG |
P397L |
XP_016856711.1 |
| XM_017001223.1 |
2254 |
Missense Mutation |
CCG,CTG |
P397L |
XP_016856712.1 |
| XM_017001224.1 |
2254 |
Missense Mutation |
CCG,CTG |
P397L |
XP_016856713.1 |
| XM_017001225.1 |
2254 |
Missense Mutation |
CCG,CTG |
P335L |
XP_016856714.1 |
- Gene
- SZRD1
- Gene Name
- SUZ RNA binding domain containing 1
There are no transcripts associated with this gene.
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