Product Details
- SNP ID
-
rs150220656
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
5
- Location
-
Chr.1:52425475 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGGGGACGCGGTGCATGTTCCCAAG[G/T]AATTGGAGGAGTCAGTCCTCGAAAG
- Phenotype
-
MIM: 617031
MIM: 613692
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
PRPF38A
PubMed Links
Gene Details
- Gene
- PRPF38A
- Gene Name
- pre-mRNA processing factor 38A
There are no transcripts associated with this gene.
- Gene
- ZCCHC11
- Gene Name
- zinc finger CCHC-type containing 11
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001009881.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1582P |
NP_001009881.1 |
NM_015269.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1581P |
NP_056084.1 |
XM_005270676.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1582P |
XP_005270733.1 |
XM_005270678.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1581P |
XP_005270735.1 |
XM_005270679.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1577P |
XP_005270736.1 |
XM_005270680.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1577P |
XP_005270737.1 |
XM_005270681.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1544P |
XP_005270738.1 |
XM_005270682.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1471P |
XP_005270739.1 |
XM_005270683.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1460P |
XP_005270740.1 |
XM_006710498.2 |
4307 |
Missense Mutation |
ACT,CCT |
T1582P |
XP_006710561.1 |
XM_006710499.3 |
4307 |
Missense Mutation |
ACT,CCT |
T1582P |
XP_006710562.1 |
XM_006710500.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1511P |
XP_006710563.1 |
XM_011541097.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1582P |
XP_011539399.1 |
XM_011541098.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1555P |
XP_011539400.1 |
XM_011541099.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1484P |
XP_011539401.1 |
XM_011541100.2 |
4307 |
Intron |
|
|
XP_011539402.1 |
XM_011541101.2 |
4307 |
Intron |
|
|
XP_011539403.1 |
XM_017000803.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1550P |
XP_016856292.1 |
XM_017000804.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1550P |
XP_016856293.1 |
XM_017000805.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1539P |
XP_016856294.1 |
XM_017000806.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1506P |
XP_016856295.1 |
XM_017000807.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1506P |
XP_016856296.1 |
XM_017000808.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1466P |
XP_016856297.1 |
XM_017000809.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1471P |
XP_016856298.1 |
XM_017000810.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1466P |
XP_016856299.1 |
XM_017000811.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1460P |
XP_016856300.1 |
XM_017000812.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1459P |
XP_016856301.1 |
XM_017000813.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1455P |
XP_016856302.1 |
XM_017000814.1 |
4307 |
Missense Mutation |
ACT,CCT |
T1349P |
XP_016856303.1 |
XM_017000815.1 |
4307 |
Intron |
|
|
XP_016856304.1 |
XM_017000816.1 |
4307 |
Intron |
|
|
XP_016856305.1 |
XM_017000817.1 |
4307 |
Intron |
|
|
XP_016856306.1 |
XM_017000818.1 |
4307 |
Intron |
|
|
XP_016856307.1 |
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