Product Details
- SNP ID
-
rs199811601
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:53109113 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTGATGTAGTGCAAGGCATGAATTT[C/T]GACTGAAGACCTTGTCACACTCATA
- Phenotype
-
MIM: 600398
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
ZNF160
PubMed Links
Gene Details
- Gene
- ZNF160
- Gene Name
- zinc finger protein 160
There are no transcripts associated with this gene.
- Gene
- ZNF415
- Gene Name
- zinc finger protein 415
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001136038.2 |
1618 |
Missense Mutation |
CAA,CGA |
Q311R |
NP_001129510.2 |
NM_001164309.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q311R |
NP_001157781.1 |
NM_018355.3 |
1618 |
Missense Mutation |
CAA,CGA |
Q311R |
NP_060825.2 |
XM_006723267.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q388R |
XP_006723330.1 |
XM_006723268.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q357R |
XP_006723331.1 |
XM_006723272.2 |
1618 |
Missense Mutation |
CAA,CGA |
Q323R |
XP_006723335.1 |
XM_006723273.2 |
1618 |
Missense Mutation |
CAA,CGA |
Q323R |
XP_006723336.1 |
XM_006723274.2 |
1618 |
Missense Mutation |
CAA,CGA |
Q323R |
XP_006723337.1 |
XM_006723277.2 |
1618 |
Missense Mutation |
CAA,CGA |
Q298R |
XP_006723340.1 |
XM_006723279.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q298R |
XP_006723342.1 |
XM_006723280.2 |
1618 |
Missense Mutation |
CAA,CGA |
Q286R |
XP_006723343.1 |
XM_006723281.2 |
1618 |
Missense Mutation |
CAA,CGA |
Q81R |
XP_006723344.1 |
XM_006723282.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q81R |
XP_006723345.1 |
XM_011527100.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q347R |
XP_011525402.1 |
XM_011527101.2 |
1618 |
Missense Mutation |
CAA,CGA |
Q347R |
XP_011525403.1 |
XM_011527103.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q311R |
XP_011525405.1 |
XM_011527104.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q298R |
XP_011525406.1 |
XM_017026952.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q347R |
XP_016882441.1 |
XM_017026953.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q388R |
XP_016882442.1 |
XM_017026954.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q388R |
XP_016882443.1 |
XM_017026955.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q359R |
XP_016882444.1 |
XM_017026956.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q359R |
XP_016882445.1 |
XM_017026957.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q359R |
XP_016882446.1 |
XM_017026958.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q359R |
XP_016882447.1 |
XM_017026959.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q359R |
XP_016882448.1 |
XM_017026960.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q359R |
XP_016882449.1 |
XM_017026961.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q349R |
XP_016882450.1 |
XM_017026962.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q347R |
XP_016882451.1 |
XM_017026963.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q347R |
XP_016882452.1 |
XM_017026964.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q311R |
XP_016882453.1 |
XM_017026965.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q311R |
XP_016882454.1 |
XM_017026966.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q311R |
XP_016882455.1 |
XM_017026967.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q311R |
XP_016882456.1 |
XM_017026968.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q298R |
XP_016882457.1 |
XM_017026969.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q282R |
XP_016882458.1 |
XM_017026970.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q323R |
XP_016882459.1 |
XM_017026971.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q339R |
XP_016882460.1 |
XM_017026972.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q81R |
XP_016882461.1 |
XM_017026973.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q323R |
XP_016882462.1 |
XM_017026974.1 |
1618 |
Missense Mutation |
CAA,CGA |
Q359R |
XP_016882463.1 |
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