Product Details

SNP ID
rs34878893
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:53109197 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGATGTAGTGCAAGGCATGAGTTG[C/T]GACTGAAACTTCTGTCACATTCATT
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 1534 Missense Mutation CAC,CGC H283R NP_001129510.2
NM_001164309.1 1534 Missense Mutation CAC,CGC H283R NP_001157781.1
NM_018355.3 1534 Missense Mutation CAC,CGC H283R NP_060825.2
XM_006723267.1 1534 Missense Mutation CAC,CGC H360R XP_006723330.1
XM_006723268.1 1534 Missense Mutation CAC,CGC H329R XP_006723331.1
XM_006723272.2 1534 Missense Mutation CAC,CGC H295R XP_006723335.1
XM_006723273.2 1534 Missense Mutation CAC,CGC H295R XP_006723336.1
XM_006723274.2 1534 Missense Mutation CAC,CGC H295R XP_006723337.1
XM_006723277.2 1534 Missense Mutation CAC,CGC H270R XP_006723340.1
XM_006723279.1 1534 Missense Mutation CAC,CGC H270R XP_006723342.1
XM_006723280.2 1534 Missense Mutation CAC,CGC H258R XP_006723343.1
XM_006723281.2 1534 Missense Mutation CAC,CGC H53R XP_006723344.1
XM_006723282.1 1534 Missense Mutation CAC,CGC H53R XP_006723345.1
XM_011527100.1 1534 Missense Mutation CAC,CGC H319R XP_011525402.1
XM_011527101.2 1534 Missense Mutation CAC,CGC H319R XP_011525403.1
XM_011527103.1 1534 Missense Mutation CAC,CGC H283R XP_011525405.1
XM_011527104.1 1534 Missense Mutation CAC,CGC H270R XP_011525406.1
XM_017026952.1 1534 Missense Mutation CAC,CGC H319R XP_016882441.1
XM_017026953.1 1534 Missense Mutation CAC,CGC H360R XP_016882442.1
XM_017026954.1 1534 Missense Mutation CAC,CGC H360R XP_016882443.1
XM_017026955.1 1534 Missense Mutation CAC,CGC H331R XP_016882444.1
XM_017026956.1 1534 Missense Mutation CAC,CGC H331R XP_016882445.1
XM_017026957.1 1534 Missense Mutation CAC,CGC H331R XP_016882446.1
XM_017026958.1 1534 Missense Mutation CAC,CGC H331R XP_016882447.1
XM_017026959.1 1534 Missense Mutation CAC,CGC H331R XP_016882448.1
XM_017026960.1 1534 Missense Mutation CAC,CGC H331R XP_016882449.1
XM_017026961.1 1534 Missense Mutation CAC,CGC H321R XP_016882450.1
XM_017026962.1 1534 Missense Mutation CAC,CGC H319R XP_016882451.1
XM_017026963.1 1534 Missense Mutation CAC,CGC H319R XP_016882452.1
XM_017026964.1 1534 Missense Mutation CAC,CGC H283R XP_016882453.1
XM_017026965.1 1534 Missense Mutation CAC,CGC H283R XP_016882454.1
XM_017026966.1 1534 Missense Mutation CAC,CGC H283R XP_016882455.1
XM_017026967.1 1534 Missense Mutation CAC,CGC H283R XP_016882456.1
XM_017026968.1 1534 Missense Mutation CAC,CGC H270R XP_016882457.1
XM_017026969.1 1534 Missense Mutation CAC,CGC H254R XP_016882458.1
XM_017026970.1 1534 Missense Mutation CAC,CGC H295R XP_016882459.1
XM_017026971.1 1534 Missense Mutation CAC,CGC H311R XP_016882460.1
XM_017026972.1 1534 Missense Mutation CAC,CGC H53R XP_016882461.1
XM_017026973.1 1534 Missense Mutation CAC,CGC H295R XP_016882462.1
XM_017026974.1 1534 Missense Mutation CAC,CGC H331R XP_016882463.1

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