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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

All alleles are reported in the Forward orientation. Click on the Variant Details tab for details on Genomic Placement, Gene, and Amino Acid changes. HGVS names are in the HGVS tab.

Reference SNP (rs) Report

This page reports data for a single dbSNP Reference SNP variation (RefSNP or rs) from the new redesigned dbSNP build.
Top of the page reports a concise summary for the rs, with more specific details included in the corresponding tabs below.
All alleles are reported in the Forward orientation. Use the Genomic View to inspect the nucleotides flanking the variant, and its neighbors.
For more information see Help documentation.

rs1485961415

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr14:23564367 (GRCh38.p14) Help

The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.

Alleles
C>G
Variation Type
SNV Single Nucleotide Variation
Frequency
G=0.000004 (1/251482, GnomAD_exome)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
AP1G2 : Missense Variant
AP1G2-AS1 : Intron Variant
Publications
0 citations
Genomic View
See rs on genome
Help

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

Download
Study Population Group Sample Size Ref Allele Alt Allele
gnomAD - Exomes Global Study-wide 251482 C=0.999996 G=0.000004
gnomAD - Exomes European Sub 135416 C=1.000000 G=0.000000
gnomAD - Exomes Asian Sub 49010 C=1.00000 G=0.00000
gnomAD - Exomes American Sub 34582 C=1.00000 G=0.00000
gnomAD - Exomes African Sub 16256 C=1.00000 G=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10078 C=1.00000 G=0.00000
gnomAD - Exomes Other Sub 6140 C=0.9998 G=0.0002
Help

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements
Sequence name Change
GRCh38.p14 chr 14 NC_000014.9:g.23564367C>G
GRCh37.p13 chr 14 NC_000014.8:g.24033576C>G
AP1G2 RefSeqGene NG_011937.1:g.8704G>C
Gene: AP1G2, adaptor related protein complex 1 subunit gamma 2 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
AP1G2 transcript variant 3 NM_001282474.2:c.-263= N/A 5 Prime UTR Variant
AP1G2 transcript variant 7 NM_001354675.2:c.-452= N/A 5 Prime UTR Variant
AP1G2 transcript variant 10 NM_001354681.2:c.-263= N/A 5 Prime UTR Variant
AP1G2 transcript variant 8 NM_001354677.2:c.-390= N/A 5 Prime UTR Variant
AP1G2 transcript variant 6 NM_001354674.2:c.-263= N/A 5 Prime UTR Variant
AP1G2 transcript variant 1 NM_003917.5:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform 1 NP_003908.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant 5 NM_001354673.2:c.556G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform 4 NP_001341602.1:p.Gly186Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant 4 NM_001282475.2:c.727G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform 3 NP_001269404.1:p.Gly243Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant 11 NR_148938.2:n.924G>C N/A Non Coding Transcript Variant
AP1G2 transcript variant 9 NR_148937.2:n.1460G>C N/A Non Coding Transcript Variant
AP1G2 transcript variant X1 XM_047431849.1:c.1216G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X1 XP_047287805.1:p.Gly406Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X2 XM_005268167.4:c.1114G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X2 XP_005268224.1:p.Gly372Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X3 XM_005268168.6:c.1114G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X2 XP_005268225.1:p.Gly372Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X4 XM_005268170.4:c.1114G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X2 XP_005268227.1:p.Gly372Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X5 XM_005268169.4:c.1114G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X2 XP_005268226.1:p.Gly372Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X6 XM_006720301.4:c.1114G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X2 XP_006720364.1:p.Gly372Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X7 XM_011537283.4:c.1216G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X3 XP_011535585.2:p.Gly406Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X8 XM_047431850.1:c.1045G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X4 XP_047287806.1:p.Gly349Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X9 XM_047431851.1:c.1114G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X5 XP_047287807.1:p.Gly372Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X10 XM_047431852.1:c.1114G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X5 XP_047287808.1:p.Gly372Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X11 XM_047431853.1:c.1114G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X5 XP_047287809.1:p.Gly372Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X12 XM_047431854.1:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X6 XP_047287810.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X13 XM_047431855.1:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X6 XP_047287811.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X14 XM_005268173.4:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X6 XP_005268230.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X15 XM_005268172.4:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X6 XP_005268229.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X16 XM_047431856.1:c.1045G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X7 XP_047287812.1:p.Gly349Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X17 XM_047431857.1:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X8 XP_047287813.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X18 XM_047431858.1:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X8 XP_047287814.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X19 XM_047431859.1:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X8 XP_047287815.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X20 XM_047431860.1:c.1216G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X9 XP_047287816.1:p.Gly406Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X21 XM_047431861.1:c.1216G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X10 XP_047287817.1:p.Gly406Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X22 XM_047431862.1:c.1216G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X11 XP_047287818.1:p.Gly406Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X23 XM_047431863.1:c.313G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X12 XP_047287819.1:p.Gly105Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X24 XM_047431864.1:c.1114G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X13 XP_047287820.1:p.Gly372Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X25 XM_047431865.1:c.1045G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X14 XP_047287821.1:p.Gly349Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X26 XM_047431866.1:c.973G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X15 XP_047287822.1:p.Gly325Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X27 XM_047431867.1:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X16 XP_047287823.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X28 XM_047431868.1:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X16 XP_047287824.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X29 XM_047431869.1:c.943G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X16 XP_047287825.1:p.Gly315Arg G (Gly) > R (Arg) Missense Variant
AP1G2 transcript variant X30 XM_047431870.1:c.1216G>C G [GGT] > R [CGT] Coding Sequence Variant
AP-1 complex subunit gamma-like 2 isoform X17 XP_047287826.1:p.Gly406Arg G (Gly) > R (Arg) Missense Variant
Gene: AP1G2-AS1, AP1G2 antisense RNA 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
AP1G2-AS1 transcript NR_110555.1:n. N/A Intron Variant
Help

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar
Help

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement C= G
GRCh38.p14 chr 14 NC_000014.9:g.23564367= NC_000014.9:g.23564367C>G
GRCh37.p13 chr 14 NC_000014.8:g.24033576= NC_000014.8:g.24033576C>G
AP1G2 RefSeqGene NG_011937.1:g.8704= NG_011937.1:g.8704G>C
AP1G2 transcript variant 1 NM_003917.5:c.943= NM_003917.5:c.943G>C
AP1G2 transcript variant 1 NM_003917.4:c.943= NM_003917.4:c.943G>C
AP1G2 transcript NM_003917.3:c.943= NM_003917.3:c.943G>C
AP1G2 transcript NM_003917.2:c.943= NM_003917.2:c.943G>C
AP1G2 transcript variant 9 NR_148937.2:n.1460= NR_148937.2:n.1460G>C
AP1G2 transcript variant 9 NR_148937.1:n.1182= NR_148937.1:n.1182G>C
AP1G2 transcript variant 8 NM_001354677.2:c.-390= NM_001354677.2:c.-390G>C
AP1G2 transcript variant 8 NM_001354677.1:c.-390= NM_001354677.1:c.-390G>C
AP1G2 transcript variant 10 NM_001354681.2:c.-263= NM_001354681.2:c.-263G>C
AP1G2 transcript variant 10 NM_001354681.1:c.-263= NM_001354681.1:c.-263G>C
AP1G2 transcript variant 11 NR_148938.2:n.924= NR_148938.2:n.924G>C
AP1G2 transcript variant 11 NR_148938.1:n.921= NR_148938.1:n.921G>C
AP1G2 transcript variant 4 NM_001282475.2:c.727= NM_001282475.2:c.727G>C
AP1G2 transcript variant 4 NM_001282475.1:c.727= NM_001282475.1:c.727G>C
AP1G2 transcript variant 3 NM_001282474.2:c.-263= NM_001282474.2:c.-263G>C
AP1G2 transcript variant 3 NM_001282474.1:c.-263= NM_001282474.1:c.-263G>C
AP1G2 transcript variant 6 NM_001354674.2:c.-263= NM_001354674.2:c.-263G>C
AP1G2 transcript variant 6 NM_001354674.1:c.-263= NM_001354674.1:c.-263G>C
AP1G2 transcript variant 7 NM_001354675.2:c.-452= NM_001354675.2:c.-452G>C
AP1G2 transcript variant 7 NM_001354675.1:c.-452= NM_001354675.1:c.-452G>C
AP1G2 transcript variant 5 NM_001354673.2:c.556= NM_001354673.2:c.556G>C
AP1G2 transcript variant 5 NM_001354673.1:c.556= NM_001354673.1:c.556G>C
AP1G2 transcript variant X3 XM_005268168.6:c.1114= XM_005268168.6:c.1114G>C
AP1G2 transcript variant X2 XM_005268168.5:c.1114= XM_005268168.5:c.1114G>C
AP1G2 transcript variant X2 XM_005268168.4:c.1114= XM_005268168.4:c.1114G>C
AP1G2 transcript variant X3 XM_005268168.3:c.1114= XM_005268168.3:c.1114G>C
AP1G2 transcript variant X3 XM_005268168.2:c.1114= XM_005268168.2:c.1114G>C
AP1G2 transcript variant X3 XM_005268168.1:c.1114= XM_005268168.1:c.1114G>C
AP1G2 transcript variant X5 XM_005268169.4:c.1114= XM_005268169.4:c.1114G>C
AP1G2 transcript variant X5 XM_005268169.3:c.1114= XM_005268169.3:c.1114G>C
AP1G2 transcript variant X5 XM_005268169.2:c.1114= XM_005268169.2:c.1114G>C
AP1G2 transcript variant X4 XM_005268169.1:c.1114= XM_005268169.1:c.1114G>C
AP1G2 transcript variant X7 XM_011537283.4:c.1216= XM_011537283.4:c.1216G>C
AP1G2 transcript variant X6 XM_011537283.3:c.1114= XM_011537283.3:c.1114G>C
AP1G2 transcript variant X6 XM_011537283.2:c.1114= XM_011537283.2:c.1114G>C
AP1G2 transcript variant X7 XM_011537283.1:c.1114= XM_011537283.1:c.1114G>C
AP1G2 transcript variant X6 XM_006720301.4:c.1114= XM_006720301.4:c.1114G>C
AP1G2 transcript variant X3 XM_006720301.3:c.1114= XM_006720301.3:c.1114G>C
AP1G2 transcript variant X6 XM_006720301.2:c.1114= XM_006720301.2:c.1114G>C
AP1G2 transcript variant X21 XM_006720301.1:c.1114= XM_006720301.1:c.1114G>C
AP1G2 transcript variant X15 XM_005268172.4:c.943= XM_005268172.4:c.943G>C
AP1G2 transcript variant X10 XM_005268172.3:c.943= XM_005268172.3:c.943G>C
AP1G2 transcript variant X9 XM_005268172.2:c.943= XM_005268172.2:c.943G>C
AP1G2 transcript variant X7 XM_005268172.1:c.943= XM_005268172.1:c.943G>C
AP1G2 transcript variant X2 XM_005268167.4:c.1114= XM_005268167.4:c.1114G>C
AP1G2 transcript variant X1 XM_005268167.3:c.1114= XM_005268167.3:c.1114G>C
AP1G2 transcript variant X1 XM_005268167.2:c.1114= XM_005268167.2:c.1114G>C
AP1G2 transcript variant X2 XM_005268167.1:c.1114= XM_005268167.1:c.1114G>C
AP1G2 transcript variant X4 XM_005268170.4:c.1114= XM_005268170.4:c.1114G>C
AP1G2 transcript variant X4 XM_005268170.3:c.1114= XM_005268170.3:c.1114G>C
AP1G2 transcript variant X4 XM_005268170.2:c.1114= XM_005268170.2:c.1114G>C
AP1G2 transcript variant X5 XM_005268170.1:c.1114= XM_005268170.1:c.1114G>C
AP1G2 transcript variant X14 XM_005268173.4:c.943= XM_005268173.4:c.943G>C
AP1G2 transcript variant X9 XM_005268173.3:c.943= XM_005268173.3:c.943G>C
AP1G2 transcript variant X8 XM_005268173.2:c.943= XM_005268173.2:c.943G>C
AP1G2 transcript variant X8 XM_005268173.1:c.943= XM_005268173.1:c.943G>C
AP1G2 transcript variant 2 NM_080545.1:c.943= NM_080545.1:c.943G>C
AP1G2 transcript variant X1 XM_047431849.1:c.1216= XM_047431849.1:c.1216G>C
AP1G2 transcript variant X12 XM_047431854.1:c.943= XM_047431854.1:c.943G>C
AP1G2 transcript variant X11 XM_047431853.1:c.1114= XM_047431853.1:c.1114G>C
AP1G2 transcript variant X8 XM_047431850.1:c.1045= XM_047431850.1:c.1045G>C
AP1G2 transcript variant X10 XM_047431852.1:c.1114= XM_047431852.1:c.1114G>C
AP1G2 transcript variant X16 XM_047431856.1:c.1045= XM_047431856.1:c.1045G>C
AP1G2 transcript variant X13 XM_047431855.1:c.943= XM_047431855.1:c.943G>C
AP1G2 transcript variant X9 XM_047431851.1:c.1114= XM_047431851.1:c.1114G>C
AP1G2 transcript variant X18 XM_047431858.1:c.943= XM_047431858.1:c.943G>C
AP1G2 transcript variant X26 XM_047431866.1:c.973= XM_047431866.1:c.973G>C
AP1G2 transcript variant X17 XM_047431857.1:c.943= XM_047431857.1:c.943G>C
AP1G2 transcript variant X19 XM_047431859.1:c.943= XM_047431859.1:c.943G>C
AP1G2 transcript variant X20 XM_047431860.1:c.1216= XM_047431860.1:c.1216G>C
AP1G2 transcript variant X21 XM_047431861.1:c.1216= XM_047431861.1:c.1216G>C
AP1G2 transcript variant X22 XM_047431862.1:c.1216= XM_047431862.1:c.1216G>C
AP1G2 transcript variant X23 XM_047431863.1:c.313= XM_047431863.1:c.313G>C
AP1G2 transcript variant X29 XM_047431869.1:c.943= XM_047431869.1:c.943G>C
AP1G2 transcript variant X25 XM_047431865.1:c.1045= XM_047431865.1:c.1045G>C
AP1G2 transcript variant X24 XM_047431864.1:c.1114= XM_047431864.1:c.1114G>C
AP1G2 transcript variant X27 XM_047431867.1:c.943= XM_047431867.1:c.943G>C
AP1G2 transcript variant X28 XM_047431868.1:c.943= XM_047431868.1:c.943G>C
AP1G2 transcript variant X30 XM_047431870.1:c.1216= XM_047431870.1:c.1216G>C
AP-1 complex subunit gamma-like 2 isoform 1 NP_003908.1:p.Gly315= NP_003908.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform 3 NP_001269404.1:p.Gly243= NP_001269404.1:p.Gly243Arg
AP-1 complex subunit gamma-like 2 isoform 4 NP_001341602.1:p.Gly186= NP_001341602.1:p.Gly186Arg
AP-1 complex subunit gamma-like 2 isoform X2 XP_005268225.1:p.Gly372= XP_005268225.1:p.Gly372Arg
AP-1 complex subunit gamma-like 2 isoform X2 XP_005268226.1:p.Gly372= XP_005268226.1:p.Gly372Arg
AP-1 complex subunit gamma-like 2 isoform X3 XP_011535585.2:p.Gly406= XP_011535585.2:p.Gly406Arg
AP-1 complex subunit gamma-like 2 isoform X2 XP_006720364.1:p.Gly372= XP_006720364.1:p.Gly372Arg
AP-1 complex subunit gamma-like 2 isoform X6 XP_005268229.1:p.Gly315= XP_005268229.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X2 XP_005268224.1:p.Gly372= XP_005268224.1:p.Gly372Arg
AP-1 complex subunit gamma-like 2 isoform X2 XP_005268227.1:p.Gly372= XP_005268227.1:p.Gly372Arg
AP-1 complex subunit gamma-like 2 isoform X6 XP_005268230.1:p.Gly315= XP_005268230.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X1 XP_047287805.1:p.Gly406= XP_047287805.1:p.Gly406Arg
AP-1 complex subunit gamma-like 2 isoform X6 XP_047287810.1:p.Gly315= XP_047287810.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X5 XP_047287809.1:p.Gly372= XP_047287809.1:p.Gly372Arg
AP-1 complex subunit gamma-like 2 isoform X4 XP_047287806.1:p.Gly349= XP_047287806.1:p.Gly349Arg
AP-1 complex subunit gamma-like 2 isoform X5 XP_047287808.1:p.Gly372= XP_047287808.1:p.Gly372Arg
AP-1 complex subunit gamma-like 2 isoform X7 XP_047287812.1:p.Gly349= XP_047287812.1:p.Gly349Arg
AP-1 complex subunit gamma-like 2 isoform X6 XP_047287811.1:p.Gly315= XP_047287811.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X5 XP_047287807.1:p.Gly372= XP_047287807.1:p.Gly372Arg
AP-1 complex subunit gamma-like 2 isoform X8 XP_047287814.1:p.Gly315= XP_047287814.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X15 XP_047287822.1:p.Gly325= XP_047287822.1:p.Gly325Arg
AP-1 complex subunit gamma-like 2 isoform X8 XP_047287813.1:p.Gly315= XP_047287813.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X8 XP_047287815.1:p.Gly315= XP_047287815.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X9 XP_047287816.1:p.Gly406= XP_047287816.1:p.Gly406Arg
AP-1 complex subunit gamma-like 2 isoform X10 XP_047287817.1:p.Gly406= XP_047287817.1:p.Gly406Arg
AP-1 complex subunit gamma-like 2 isoform X11 XP_047287818.1:p.Gly406= XP_047287818.1:p.Gly406Arg
AP-1 complex subunit gamma-like 2 isoform X12 XP_047287819.1:p.Gly105= XP_047287819.1:p.Gly105Arg
AP-1 complex subunit gamma-like 2 isoform X16 XP_047287825.1:p.Gly315= XP_047287825.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X14 XP_047287821.1:p.Gly349= XP_047287821.1:p.Gly349Arg
AP-1 complex subunit gamma-like 2 isoform X13 XP_047287820.1:p.Gly372= XP_047287820.1:p.Gly372Arg
AP-1 complex subunit gamma-like 2 isoform X16 XP_047287823.1:p.Gly315= XP_047287823.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X16 XP_047287824.1:p.Gly315= XP_047287824.1:p.Gly315Arg
AP-1 complex subunit gamma-like 2 isoform X17 XP_047287826.1:p.Gly406= XP_047287826.1:p.Gly406Arg
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Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

1 SubSNP, 1 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2740614203 Nov 08, 2017 (151)
2 gnomAD - Exomes NC_000014.8 - 24033576 Jul 13, 2019 (153)
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History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:
Submission IDs Observation SPDI Canonical SPDI Source RSIDs
9863406, ss2740614203 NC_000014.8:24033575:C:G NC_000014.9:23564366:C:G (self)
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Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs1485961415

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The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:
Select flank length:

Genomic regions, transcripts, and products
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NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

Software version is: 2.0.1.post820+afb47a3d