Product Details

SNP ID
rs147119635
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:28955728 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTATGTTCTTCCCACAGGTAGATG[A/C]CCCCTGACATGGGCCCAATGAAGGG
Phenotype
MIM: 616666
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
PHF12 PubMed Links

Gene Details

Gene
PHF12
Gene Name
PHD finger protein 12
There are no transcripts associated with this gene.

Gene
SEZ6
Gene Name
seizure related 6 homolog
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001098635.1 3310 UTR 3 NP_001092105.1
NM_001290202.1 3310 UTR 3 NP_001277131.1
NM_178860.4 3310 UTR 3 NP_849191.3
XM_011524315.1 3310 Missense Mutation XP_011522617.1
XM_011524317.2 3310 UTR 3 XP_011522619.1

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