Product Details
- SNP ID
-
rs199739678
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.7:150371414 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCCCAAGCCCCAGGCAGGGCCCATC[A/G]CTGTGCCCACTGTCGAAGGCACTTC
- Phenotype
-
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
REPIN1
PubMed Links
Gene Details
- Gene
- REPIN1
- Gene Name
- replication initiator 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001099695.1 |
246 |
Missense Mutation |
CAC,CGC |
H115R |
NP_001093165.1 |
NM_001099696.2 |
246 |
Missense Mutation |
CAC,CGC |
H58R |
NP_001093166.1 |
NM_013400.3 |
246 |
Missense Mutation |
CAC,CGC |
H58R |
NP_037532.2 |
NM_014374.3 |
246 |
Missense Mutation |
CAC,CGC |
H58R |
NP_055189.2 |
XM_005249985.1 |
246 |
Missense Mutation |
CAC,CGC |
H58R |
XP_005250042.1 |
XM_006715947.3 |
246 |
Missense Mutation |
CAC,CGC |
H115R |
XP_006716010.1 |
XM_006715948.3 |
246 |
Missense Mutation |
CAC,CGC |
H115R |
XP_006716011.1 |
XM_006715949.3 |
246 |
Missense Mutation |
CAC,CGC |
H115R |
XP_006716012.1 |
XM_006715950.3 |
246 |
Missense Mutation |
CAC,CGC |
H114R |
XP_006716013.1 |
XM_006715951.2 |
246 |
Missense Mutation |
CAC,CGC |
H114R |
XP_006716014.1 |
XM_006715952.2 |
246 |
Missense Mutation |
CAC,CGC |
H58R |
XP_006716015.1 |
XM_006715953.2 |
246 |
Missense Mutation |
CAC,CGC |
H58R |
XP_006716016.1 |
XM_011516112.1 |
246 |
Missense Mutation |
CAC,CGC |
H58R |
XP_011514414.1 |
XM_017012081.1 |
246 |
Missense Mutation |
CAC,CGC |
H58R |
XP_016867570.1 |
XM_017012082.1 |
246 |
Missense Mutation |
CAC,CGC |
H58R |
XP_016867571.1 |
- Gene
- ZNF775
- Gene Name
- zinc finger protein 775
There are no transcripts associated with this gene.
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