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dbSNP Short Genetic Variations

Examples: rs268, BRCA1 and more Advanced search

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.

rs1466168256

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr5:141510980 (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
G>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000004 (1/248860, GnomAD_exome)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
PCDHGA1 : Missense Variant
PCDHGA10 : Missense Variant
PCDHGA11 : Missense Variant (+ 19 more)
PCDHGA12 : Missense Variant
PCDHGA2 : Missense Variant
PCDHGA3 : Missense Variant
PCDHGA4 : Missense Variant
PCDHGA5 : Missense Variant
PCDHGA6 : Missense Variant
PCDHGA7 : Missense Variant
PCDHGA8 : Missense Variant
PCDHGA9 : Missense Variant
PCDHGB1 : Missense Variant
PCDHGB2 : Missense Variant
PCDHGB3 : Missense Variant
PCDHGB4 : Missense Variant
PCDHGB5 : Missense Variant
PCDHGB6 : Missense Variant
PCDHGB7 : Missense Variant
PCDHGC3 : Missense Variant
PCDHGC4 : Missense Variant
PCDHGC5 : Missense 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 248860 G=0.999996 C=0.000004
gnomAD - Exomes European Sub 132872 G=0.999992 C=0.000008
gnomAD - Exomes Asian Sub 49006 G=1.00000 C=0.00000
gnomAD - Exomes American Sub 34582 G=1.00000 C=0.00000
gnomAD - Exomes African Sub 16216 G=1.00000 C=0.00000
gnomAD - Exomes Ashkenazi Jewish Sub 10064 G=1.00000 C=0.00000
gnomAD - Exomes Other Sub 6120 G=1.0000 C=0.0000
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 5 NC_000005.10:g.141510980G>C
GRCh37.p13 chr 5 NC_000005.9:g.140890547G>C
PCDHG genomic region NG_000012.2:g.221177G>C
PCDHGC4 RefSeqGene NG_050746.1:g.30807G>C
Gene: PCDHGB6, protocadherin gamma subfamily B, 6 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGB6 transcript variant 3 NM_001386906.1:c. N/A Genic Downstream Transcript Variant
PCDHGB6 transcript variant 2 NM_032100.1:c. N/A Genic Downstream Transcript Variant
PCDHGB6 transcript variant 1 NM_018926.3:c.2600G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-B6 isoform 1 precursor NP_061749.1:p.Gly867Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA8, protocadherin gamma subfamily A, 8 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA8 transcript variant 2 NM_014004.3:c. N/A Genic Downstream Transcript Variant
PCDHGA8 transcript variant 1 NM_032088.2:c.2606G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A8 isoform 1 precursor NP_114477.1:p.Gly869Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA1, protocadherin gamma subfamily A, 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA1 transcript variant 2 NM_031993.2:c. N/A Genic Downstream Transcript Variant
PCDHGA1 transcript variant 1 NM_018912.3:c.2603G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A1 isoform 1 precursor NP_061735.1:p.Gly868Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA2, protocadherin gamma subfamily A, 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA2 transcript variant 2 NM_032009.3:c. N/A Genic Downstream Transcript Variant
PCDHGA2 transcript variant 1 NM_018915.4:c.2606G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A2 isoform 1 precursor NP_061738.1:p.Gly869Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA3, protocadherin gamma subfamily A, 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA3 transcript variant 2 NM_032011.2:c. N/A Genic Downstream Transcript Variant
PCDHGA3 transcript variant 1 NM_018916.4:c.2606G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A3 isoform 1 precursor NP_061739.2:p.Gly869Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA4, protocadherin gamma subfamily A, 4 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA4 transcript variant 2 NM_032053.3:c. N/A Genic Downstream Transcript Variant
PCDHGA4 transcript variant 1 NM_018917.4:c.2696G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A4 isoform 1 precursor NP_061740.2:p.Gly899Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA5, protocadherin gamma subfamily A, 5 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA5 transcript variant 2 NM_032054.2:c. N/A Genic Downstream Transcript Variant
PCDHGA5 transcript variant 1 NM_018918.3:c.2603G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A5 isoform 1 precursor NP_061741.1:p.Gly868Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA6, protocadherin gamma subfamily A, 6 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA6 transcript variant 2 NM_032086.2:c. N/A Genic Downstream Transcript Variant
PCDHGA6 transcript variant 1 NM_018919.3:c.2606G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A6 isoform 1 precursor NP_061742.1:p.Gly869Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA7, protocadherin gamma subfamily A, 7 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA7 transcript variant 2 NM_032087.3:c. N/A Genic Downstream Transcript Variant
PCDHGA7 transcript variant 1 NM_018920.4:c.2606G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A7 isoform 1 precursor NP_061743.1:p.Gly869Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA9, protocadherin gamma subfamily A, 9 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA9 transcript variant 2 NM_032089.2:c. N/A Genic Downstream Transcript Variant
PCDHGA9 transcript variant 1 NM_018921.3:c.2606G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A9 isoform 1 precursor NP_061744.1:p.Gly869Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA10, protocadherin gamma subfamily A, 10 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA10 transcript variant 2 NM_032090.2:c. N/A Genic Downstream Transcript Variant
PCDHGA10 transcript variant 1 NM_018913.3:c.2618G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A10 isoform 1 precursor NP_061736.1:p.Gly873Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA11, protocadherin gamma subfamily A, 11 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA11 transcript variant 2 NM_032091.2:c. N/A Genic Downstream Transcript Variant
PCDHGA11 transcript variant 1 NM_018914.3:c.2615G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A11 isoform 1 precursor NP_061737.1:p.Gly872Ala G (Gly) > A (Ala) Missense Variant
PCDHGA11 transcript variant 3 NM_032092.2:c.2060G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A11 isoform 3 precursor NP_114481.1:p.Gly687Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGA12, protocadherin gamma subfamily A, 12 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGA12 transcript variant 2 NM_032094.2:c. N/A Genic Downstream Transcript Variant
PCDHGA12 transcript variant 1 NM_003735.3:c.2606G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-A12 isoform 1 precursor NP_003726.1:p.Gly869Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGB1, protocadherin gamma subfamily B, 1 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGB1 transcript variant 2 NM_032095.1:c. N/A Genic Downstream Transcript Variant
PCDHGB1 transcript variant 1 NM_018922.3:c.2591G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-B1 isoform 1 precursor NP_061745.1:p.Gly864Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGB2, protocadherin gamma subfamily B, 2 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGB2 transcript variant 2 NM_032096.1:c. N/A Genic Downstream Transcript Variant
PCDHGB2 transcript variant 1 NM_018923.3:c.2603G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-B2 isoform 1 precursor NP_061746.1:p.Gly868Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGB3, protocadherin gamma subfamily B, 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGB3 transcript variant 2 NM_032097.3:c. N/A Genic Downstream Transcript Variant
PCDHGB3 transcript variant 1 NM_018924.5:c.2597G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-B3 isoform 1 precursor NP_061747.2:p.Gly866Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGB4, protocadherin gamma subfamily B, 4 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGB4 transcript variant 2 NM_032098.1:c. N/A Genic Downstream Transcript Variant
PCDHGB4 transcript variant 1 NM_003736.4:c.2579G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-B4 isoform 1 precursor NP_003727.1:p.Gly860Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGB5, protocadherin gamma subfamily B, 5 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGB5 transcript variant 2 NM_032099.1:c. N/A Genic Downstream Transcript Variant
PCDHGB5 transcript variant 1 NM_018925.3:c.2579G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-B5 isoform 1 precursor NP_061748.1:p.Gly860Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGB7, protocadherin gamma subfamily B, 7 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGB7 transcript variant 2 NM_032101.3:c. N/A Genic Downstream Transcript Variant
PCDHGB7 transcript variant 1 NM_018927.4:c.2597G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-B7 isoform 1 precursor NP_061750.1:p.Gly866Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGC3, protocadherin gamma subfamily C, 3 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGC3 transcript variant 2 NM_032402.2:c. N/A Genic Downstream Transcript Variant
PCDHGC3 transcript variant 1 NM_002588.4:c.2612G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-C3 isoform 1 precursor NP_002579.2:p.Gly871Ala G (Gly) > A (Ala) Missense Variant
PCDHGC3 transcript variant 3 NM_032403.3:c.212G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-C3 isoform 3 NP_115779.1:p.Gly71Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGC4, protocadherin gamma subfamily C, 4 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGC4 transcript variant 2 NM_032406.1:c. N/A Genic Downstream Transcript Variant
PCDHGC4 transcript variant 1 NM_018928.3:c.2624G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-C4 isoform 1 precursor NP_061751.1:p.Gly875Ala G (Gly) > A (Ala) Missense Variant
PCDHGC4 transcript variant 4 NM_001386884.1:c.194G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-C4 isoform 4 NP_001373813.1:p.Gly65Ala G (Gly) > A (Ala) Missense Variant
Gene: PCDHGC5, protocadherin gamma subfamily C, 5 (plus strand)
Molecule type Change Amino acid[Codon] SO Term
PCDHGC5 transcript variant 2 NM_032407.1:c. N/A Genic Downstream Transcript Variant
PCDHGC5 transcript variant 1 NM_018929.3:c.2642G>C G [GGT] > A [GCT] Coding Sequence Variant
protocadherin gamma-C5 isoform 1 precursor NP_061752.1:p.Gly881Ala G (Gly) > A (Ala) Missense 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 G= C
GRCh38.p14 chr 5 NC_000005.10:g.141510980= NC_000005.10:g.141510980G>C
GRCh37.p13 chr 5 NC_000005.9:g.140890547= NC_000005.9:g.140890547G>C
PCDHG genomic region NG_000012.2:g.221177= NG_000012.2:g.221177G>C
PCDHGC4 RefSeqGene NG_050746.1:g.30807= NG_050746.1:g.30807G>C
PCDHGC4 transcript variant 1 NM_018928.3:c.2624= NM_018928.3:c.2624G>C
PCDHGC4 transcript variant 1 NM_018928.2:c.2624= NM_018928.2:c.2624G>C
PCDHGC4 transcript variant 4 NM_001386884.1:c.194= NM_001386884.1:c.194G>C
PCDHGB3 transcript variant 1 NM_018924.5:c.2597= NM_018924.5:c.2597G>C
PCDHGB3 transcript variant 1 NM_018924.4:c.2597= NM_018924.4:c.2597G>C
PCDHGB3 transcript variant 1 NM_018924.3:c.2597= NM_018924.3:c.2597G>C
PCDHGB3 transcript variant 1 NM_018924.2:c.2597= NM_018924.2:c.2597G>C
PCDHGA2 transcript variant 1 NM_018915.4:c.2606= NM_018915.4:c.2606G>C
PCDHGA2 transcript variant 1 NM_018915.3:c.2606= NM_018915.3:c.2606G>C
PCDHGA2 transcript variant 1 NM_018915.2:c.2606= NM_018915.2:c.2606G>C
PCDHGA3 transcript variant 1 NM_018916.4:c.2606= NM_018916.4:c.2606G>C
PCDHGA3 transcript variant 1 NM_018916.3:c.2606= NM_018916.3:c.2606G>C
PCDHGA4 transcript variant 1 NM_018917.4:c.2696= NM_018917.4:c.2696G>C
PCDHGA4 transcript variant 1 NM_018917.3:c.2696= NM_018917.3:c.2696G>C
PCDHGA4 transcript variant 1 NM_018917.2:c.2603= NM_018917.2:c.2603G>C
PCDHGB7 transcript variant 1 NM_018927.4:c.2597= NM_018927.4:c.2597G>C
PCDHGB7 transcript variant 1 NM_018927.3:c.2597= NM_018927.3:c.2597G>C
PCDHGB4 transcript variant 1 NM_003736.4:c.2579= NM_003736.4:c.2579G>C
PCDHGB4 transcript variant 1 NM_003736.3:c.2579= NM_003736.3:c.2579G>C
PCDHGB4 transcript variant 1 NM_003736.2:c.2579= NM_003736.2:c.2579G>C
PCDHGA7 transcript variant 1 NM_018920.4:c.2606= NM_018920.4:c.2606G>C
PCDHGA7 transcript variant 1 NM_018920.3:c.2606= NM_018920.3:c.2606G>C
PCDHGA7 transcript variant 1 NM_018920.2:c.2606= NM_018920.2:c.2606G>C
PCDHGC3 transcript variant 1 NM_002588.4:c.2612= NM_002588.4:c.2612G>C
PCDHGC3 transcript variant 1 NM_002588.3:c.2612= NM_002588.3:c.2612G>C
PCDHGC3 transcript variant 1 NM_002588.2:c.2612= NM_002588.2:c.2612G>C
PCDHGA12 transcript variant 1 NM_003735.3:c.2606= NM_003735.3:c.2606G>C
PCDHGA12 transcript variant 1 NM_003735.2:c.2606= NM_003735.2:c.2606G>C
PCDHGA10 transcript variant 1 NM_018913.3:c.2618= NM_018913.3:c.2618G>C
PCDHGA10 transcript variant 1 NM_018913.2:c.2618= NM_018913.2:c.2618G>C
PCDHGC5 transcript variant 1 NM_018929.3:c.2642= NM_018929.3:c.2642G>C
PCDHGC5 transcript variant 1 NM_018929.2:c.2642= NM_018929.2:c.2642G>C
PCDHGA6 transcript variant 1 NM_018919.3:c.2606= NM_018919.3:c.2606G>C
PCDHGA6 transcript variant 1 NM_018919.2:c.2606= NM_018919.2:c.2606G>C
PCDHGA11 transcript variant 1 NM_018914.3:c.2615= NM_018914.3:c.2615G>C
PCDHGA11 transcript variant 1 NM_018914.2:c.2615= NM_018914.2:c.2615G>C
PCDHGB6 transcript variant 1 NM_018926.3:c.2600= NM_018926.3:c.2600G>C
PCDHGB6 transcript variant 1 NM_018926.2:c.2600= NM_018926.2:c.2600G>C
PCDHGA9 transcript variant 1 NM_018921.3:c.2606= NM_018921.3:c.2606G>C
PCDHGA9 transcript variant 1 NM_018921.2:c.2606= NM_018921.2:c.2606G>C
PCDHGA1 transcript variant 1 NM_018912.3:c.2603= NM_018912.3:c.2603G>C
PCDHGA1 transcript variant 1 NM_018912.2:c.2603= NM_018912.2:c.2603G>C
PCDHGA5 transcript variant 1 NM_018918.3:c.2603= NM_018918.3:c.2603G>C
PCDHGA5 transcript variant 1 NM_018918.2:c.2603= NM_018918.2:c.2603G>C
PCDHGB5 transcript variant 1 NM_018925.3:c.2579= NM_018925.3:c.2579G>C
PCDHGB5 transcript variant 1 NM_018925.2:c.2579= NM_018925.2:c.2579G>C
PCDHGB1 transcript variant 1 NM_018922.3:c.2591= NM_018922.3:c.2591G>C
PCDHGB1 transcript variant 1 NM_018922.2:c.2591= NM_018922.2:c.2591G>C
PCDHGB2 transcript variant 1 NM_018923.3:c.2603= NM_018923.3:c.2603G>C
PCDHGB2 transcript variant 1 NM_018923.2:c.2603= NM_018923.2:c.2603G>C
PCDHGC3 transcript variant 3 NM_032403.3:c.212= NM_032403.3:c.212G>C
PCDHGC3 transcript variant 3 NM_032403.2:c.212= NM_032403.2:c.212G>C
PCDHGC3 transcript variant 3 NM_032403.1:c.212= NM_032403.1:c.212G>C
PCDHGA8 transcript variant 1 NM_032088.2:c.2606= NM_032088.2:c.2606G>C
PCDHGA8 transcript variant 1 NM_032088.1:c.2606= NM_032088.1:c.2606G>C
PCDHGA11 transcript variant 3 NM_032092.2:c.2060= NM_032092.2:c.2060G>C
PCDHGA11 transcript variant 3 NM_032092.1:c.2060= NM_032092.1:c.2060G>C
protocadherin gamma-C4 isoform 1 precursor NP_061751.1:p.Gly875= NP_061751.1:p.Gly875Ala
protocadherin gamma-C4 isoform 4 NP_001373813.1:p.Gly65= NP_001373813.1:p.Gly65Ala
protocadherin gamma-B3 isoform 1 precursor NP_061747.2:p.Gly866= NP_061747.2:p.Gly866Ala
protocadherin gamma-A2 isoform 1 precursor NP_061738.1:p.Gly869= NP_061738.1:p.Gly869Ala
protocadherin gamma-A3 isoform 1 precursor NP_061739.2:p.Gly869= NP_061739.2:p.Gly869Ala
protocadherin gamma-A4 isoform 1 precursor NP_061740.2:p.Gly899= NP_061740.2:p.Gly899Ala
protocadherin gamma-B7 isoform 1 precursor NP_061750.1:p.Gly866= NP_061750.1:p.Gly866Ala
protocadherin gamma-B4 isoform 1 precursor NP_003727.1:p.Gly860= NP_003727.1:p.Gly860Ala
protocadherin gamma-A7 isoform 1 precursor NP_061743.1:p.Gly869= NP_061743.1:p.Gly869Ala
protocadherin gamma-C3 isoform 1 precursor NP_002579.2:p.Gly871= NP_002579.2:p.Gly871Ala
protocadherin gamma-A12 isoform 1 precursor NP_003726.1:p.Gly869= NP_003726.1:p.Gly869Ala
protocadherin gamma-A10 isoform 1 precursor NP_061736.1:p.Gly873= NP_061736.1:p.Gly873Ala
protocadherin gamma-C5 isoform 1 precursor NP_061752.1:p.Gly881= NP_061752.1:p.Gly881Ala
protocadherin gamma-A6 isoform 1 precursor NP_061742.1:p.Gly869= NP_061742.1:p.Gly869Ala
protocadherin gamma-A11 isoform 1 precursor NP_061737.1:p.Gly872= NP_061737.1:p.Gly872Ala
protocadherin gamma-B6 isoform 1 precursor NP_061749.1:p.Gly867= NP_061749.1:p.Gly867Ala
protocadherin gamma-A9 isoform 1 precursor NP_061744.1:p.Gly869= NP_061744.1:p.Gly869Ala
protocadherin gamma-A1 isoform 1 precursor NP_061735.1:p.Gly868= NP_061735.1:p.Gly868Ala
protocadherin gamma-A5 isoform 1 precursor NP_061741.1:p.Gly868= NP_061741.1:p.Gly868Ala
protocadherin gamma-B5 isoform 1 precursor NP_061748.1:p.Gly860= NP_061748.1:p.Gly860Ala
protocadherin gamma-B1 isoform 1 precursor NP_061745.1:p.Gly864= NP_061745.1:p.Gly864Ala
protocadherin gamma-B2 isoform 1 precursor NP_061746.1:p.Gly868= NP_061746.1:p.Gly868Ala
protocadherin gamma-C3 isoform 3 NP_115779.1:p.Gly71= NP_115779.1:p.Gly71Ala
protocadherin gamma-A8 isoform 1 precursor NP_114477.1:p.Gly869= NP_114477.1:p.Gly869Ala
protocadherin gamma-A11 isoform 3 precursor NP_114481.1:p.Gly687= NP_114481.1:p.Gly687Ala
protocadherin gamma-A4 isoform 1 precursor NP_061740.1:p.Gly868= NP_061740.1:p.Gly868Ala
protocadherin gamma-B3 isoform 1 precursor NP_061747.1:p.Gly866= NP_061747.1:p.Gly866Ala
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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 ss2735312123 Nov 08, 2017 (151)
2 gnomAD - Exomes NC_000005.9 - 140890547 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
4442015, ss2735312123 NC_000005.9:140890546:G:C NC_000005.10:141510979:G:C (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 rs1466168256

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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