Product Details

SNP ID
rs2379049
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:156603 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAAGTTCTAATCACAAAGATGTTAT[A/G]TACTTTAGCTTAAAGGCCCTTATTA
Phenotype
MIM: 608668
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
ZMYND11 PubMed Links

Gene Details

Gene
ZMYND11
Gene Name
zinc finger MYND-type containing 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001202464.1 Intron NP_001189393.1
NM_001202465.1 Intron NP_001189394.1
NM_001202466.1 Intron NP_001189395.1
NM_001202467.1 Intron NP_001189396.1
NM_001202468.1 Intron NP_001189397.1
NM_006624.5 Intron NP_006615.2
NM_212479.3 Intron NP_997644.2
XM_005252359.4 Intron XP_005252416.1
XM_005252361.3 Intron XP_005252418.1
XM_005252362.2 Intron XP_005252419.1
XM_006717376.2 Intron XP_006717439.1
XM_017015587.1 Intron XP_016871076.1
XM_017015588.1 Intron XP_016871077.1
XM_017015589.1 Intron XP_016871078.1
XM_017015590.1 Intron XP_016871079.1
XM_017015591.1 Intron XP_016871080.1
XM_017015592.1 Intron XP_016871081.1
XM_017015593.1 Intron XP_016871082.1
XM_017015594.1 Intron XP_016871083.1

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