Product Details

SNP ID
rs199856439
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.4:2271758 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCACAGTGCACAGTCCTCCAAGGCC[A/G]CACTCCGCAGAGTCTGGGTGACTAG
Phenotype
MIM: 614176
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
MXD4 PubMed Links

Gene Details

Gene
MXD4
Gene Name
MAX dimerization protein 4
There are no transcripts associated with this gene.

Gene
ZFYVE28
Gene Name
zinc finger FYVE-type containing 28
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001172656.1 2719 Missense Mutation GCG,GTG A752V NP_001166127.1
NM_001172657.1 2719 Intron NP_001166128.1
NM_001172658.1 2719 Intron NP_001166129.1
NM_001172659.1 2719 Missense Mutation GCG,GTG A712V NP_001166130.1
NM_001172660.1 2719 Intron NP_001166131.1
NM_020972.2 2719 Missense Mutation GCG,GTG A782V NP_066023.2
XM_006713900.3 2719 Missense Mutation GCG,GTG A782V XP_006713963.1
XM_006713902.3 2719 Missense Mutation CGG,TGG R856W XP_006713965.1
XM_006713904.3 2719 Intron XP_006713967.1
XM_011513540.2 2719 Missense Mutation GCG,GTG A668V XP_011511842.1
XM_011513541.2 2719 Intron XP_011511843.1
XM_017008502.1 2719 Missense Mutation GCG,GTG A724V XP_016863991.1
XM_017008503.1 2719 Missense Mutation CGG,TGG R857W XP_016863992.1
XM_017008504.1 2719 Missense Mutation CGG,TGG R857W XP_016863993.1
XM_017008505.1 2719 Missense Mutation GCG,GTG A668V XP_016863994.1
XM_017008506.1 2719 Intron XP_016863995.1
XM_017008507.1 2719 Intron XP_016863996.1
XM_017008508.1 2719 Intron XP_016863997.1
XM_017008509.1 2719 Intron XP_016863998.1
XM_017008510.1 2719 Intron XP_016863999.1

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