Product Details

SNP ID
rs145378054
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:25075520 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATAAATAAATGGCAAAGGAAACGCA[A/G]GAAAGGAAAGATTTACAAAATCCAA
Phenotype
MIM: 605020
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
VSX1 PubMed Links

Gene Details

Gene
VSX1
Gene Name
visual system homeobox 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001256271.1 2122 Intron NP_001243200.1
NM_001256272.1 2122 Intron NP_001243201.1
NM_014588.5 2122 UTR 3 NP_055403.2
NM_199425.2 2122 Intron NP_955457.1
XM_017027837.1 2122 Intron XP_016883326.1
XM_017027838.1 2122 Intron XP_016883327.1

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