Product Details

SNP ID
rs191255462
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:47448719 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCACTGCATTTGTAGGGTTTCTGCC[C/T]GGTATGAATTTTTTGATGTGTAATG
Phenotype
MIM: 314995
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
ZNF41 PubMed Links

Gene Details

Gene
ZNF41
Gene Name
zinc finger protein 41
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001324139.1 1818 Missense Mutation AGG,GGG R265G NP_001311068.1
NM_001324140.1 1818 Missense Mutation AGG,GGG R351G NP_001311069.1
NM_001324141.1 1818 Missense Mutation AGG,GGG R265G NP_001311070.1
NM_001324142.1 1818 Missense Mutation AGG,GGG R353G NP_001311071.1
NM_001324143.1 1818 Missense Mutation AGG,GGG R265G NP_001311072.1
NM_001324144.1 1818 Missense Mutation AGG,GGG R351G NP_001311073.1
NM_001324145.1 1818 Missense Mutation AGG,GGG R265G NP_001311074.1
NM_001324147.1 1818 Missense Mutation AGG,GGG R351G NP_001311076.1
NM_001324148.1 1818 Missense Mutation AGG,GGG R353G NP_001311077.1
NM_001324149.1 1818 Missense Mutation AGG,GGG R265G NP_001311078.1
NM_001324150.1 1818 Missense Mutation AGG,GGG R351G NP_001311079.1
NM_001324151.1 1818 Missense Mutation AGG,GGG R361G NP_001311080.1
NM_001324152.1 1818 Missense Mutation AGG,GGG R265G NP_001311081.1
NM_001324153.1 1818 Missense Mutation AGG,GGG R361G NP_001311082.1
NM_001324154.1 1818 Missense Mutation AGG,GGG R385G NP_001311083.1
NM_001324155.1 1818 Missense Mutation AGG,GGG R393G NP_001311084.1
NM_001324156.1 1818 Missense Mutation AGG,GGG R317G NP_001311085.1
NM_001324157.1 1818 Missense Mutation AGG,GGG R315G NP_001311086.1
NM_007130.3 1818 Missense Mutation AGG,GGG R351G NP_009061.1
NM_153380.3 1818 Missense Mutation AGG,GGG R351G NP_700359.1
XM_006724550.3 1818 Missense Mutation AGG,GGG R385G XP_006724613.1
XM_006724555.3 1818 Missense Mutation AGG,GGG R361G XP_006724618.1
XM_017029810.1 1818 Missense Mutation AGG,GGG R385G XP_016885299.1
XM_017029811.1 1818 Missense Mutation AGG,GGG R385G XP_016885300.1
XM_017029812.1 1818 Missense Mutation AGG,GGG R385G XP_016885301.1
XM_017029813.1 1818 Missense Mutation AGG,GGG R385G XP_016885302.1
XM_017029814.1 1818 Missense Mutation AGG,GGG R385G XP_016885303.1
XM_017029815.1 1818 Missense Mutation AGG,GGG R385G XP_016885304.1
XM_017029816.1 1818 Missense Mutation AGG,GGG R361G XP_016885305.1
XM_017029817.1 1818 Missense Mutation AGG,GGG R351G XP_016885306.1

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