Product Details
- SNP ID
-
rs150967108
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.5:79619674 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ATGTTCCCAAACTCAATTTTGGGTC[A/G]CCCACCCTTCACTCCAAATCATCAA
- Phenotype
-
MIM: 614121
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
PAPD4
PubMed Links
Gene Details
- Gene
- PAPD4
- Gene Name
- PAP associated domain containing 4
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001114393.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
NP_001107865.1 |
NM_001114394.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
NP_001107866.1 |
NM_001297744.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
NP_001284673.1 |
NM_001297745.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
NP_001284674.1 |
NM_173797.3 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
NP_776158.2 |
XM_011543219.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541521.1 |
XM_011543220.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541522.1 |
XM_011543221.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541523.1 |
XM_011543222.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541524.1 |
XM_011543223.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541525.1 |
XM_011543224.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541526.1 |
XM_011543225.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541527.1 |
XM_011543226.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541528.1 |
XM_011543227.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541529.1 |
XM_011543228.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541530.1 |
XM_011543229.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541531.1 |
XM_011543230.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541532.1 |
XM_011543231.2 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_011541533.1 |
XM_011543232.2 |
870 |
Intron |
|
|
XP_011541534.1 |
XM_011543233.2 |
870 |
Intron |
|
|
XP_011541535.1 |
XM_017009151.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864640.1 |
XM_017009152.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864641.1 |
XM_017009153.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864642.1 |
XM_017009154.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864643.1 |
XM_017009155.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864644.1 |
XM_017009156.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864645.1 |
XM_017009157.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864646.1 |
XM_017009158.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864647.1 |
XM_017009159.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864648.1 |
XM_017009160.1 |
870 |
Missense Mutation |
CAC,CGC |
H9R |
XP_016864649.1 |
XM_017009161.1 |
870 |
UTR 5 |
|
|
XP_016864650.1 |
XM_017009162.1 |
870 |
UTR 5 |
|
|
XP_016864651.1 |
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