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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.

rs1479981404

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chr20:46503091 (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
T>A / T>C
Variation Type
SNV Single Nucleotide Variation
Frequency
None
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ZNF334 : 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").

None
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 20 NC_000020.11:g.46503091T>A
GRCh38.p14 chr 20 NC_000020.11:g.46503091T>C
GRCh37.p13 chr 20 NC_000020.10:g.45131730T>A
GRCh37.p13 chr 20 NC_000020.10:g.45131730T>C
Gene: ZNF334, zinc finger protein 334 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ZNF334 transcript variant 6 NM_001353815.2:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340744.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 6 NM_001353815.2:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340744.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 3 NM_001270497.3:c.245A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform c NP_001257426.1:p.Asp82Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 3 NM_001270497.3:c.245A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform c NP_001257426.1:p.Asp82Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 10 NM_001353819.2:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340748.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 10 NM_001353819.2:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340748.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 2 NM_199441.3:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_955473.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 2 NM_199441.3:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_955473.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 14 NM_001353823.2:c.245A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform c NP_001340752.1:p.Asp82Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 14 NM_001353823.2:c.245A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform c NP_001340752.1:p.Asp82Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 9 NM_001353818.2:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340747.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 9 NM_001353818.2:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340747.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 12 NM_001353821.2:c.245A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform c NP_001340750.1:p.Asp82Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 12 NM_001353821.2:c.245A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform c NP_001340750.1:p.Asp82Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 15 NM_001353824.2:c.248A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform a NP_001340753.1:p.Asp83Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 15 NM_001353824.2:c.248A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform a NP_001340753.1:p.Asp83Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 7 NM_001353816.2:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340745.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 7 NM_001353816.2:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340745.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 1 NM_018102.6:c.248A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform a NP_060572.3:p.Asp83Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 1 NM_018102.6:c.248A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform a NP_060572.3:p.Asp83Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 16 NM_001353825.2:c.317A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform e NP_001340754.1:p.Asp106Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 16 NM_001353825.2:c.317A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform e NP_001340754.1:p.Asp106Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 4 NM_001353813.2:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340742.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 4 NM_001353813.2:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340742.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 11 NM_001353820.2:c.233A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform d NP_001340749.1:p.Asp78Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 11 NM_001353820.2:c.233A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform d NP_001340749.1:p.Asp78Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 8 NM_001353817.2:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340746.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 8 NM_001353817.2:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340746.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 17 NM_001353826.2:c.269A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform f NP_001340755.1:p.Asp90Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 17 NM_001353826.2:c.269A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform f NP_001340755.1:p.Asp90Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 5 NM_001353814.2:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340743.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 5 NM_001353814.2:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform b NP_001340743.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant 13 NM_001353822.2:c.245A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform c NP_001340751.1:p.Asp82Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant 13 NM_001353822.2:c.245A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform c NP_001340751.1:p.Asp82Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant X1 XM_047440279.1:c.317A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform X1 XP_047296235.1:p.Asp106Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant X1 XM_047440279.1:c.317A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform X1 XP_047296235.1:p.Asp106Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant X3 XM_047440280.1:c.269A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform X2 XP_047296236.1:p.Asp90Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant X3 XM_047440280.1:c.269A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform X2 XP_047296236.1:p.Asp90Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant X4 XM_017027937.2:c.317A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform X3 XP_016883426.1:p.Asp106Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant X4 XM_017027937.2:c.317A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform X3 XP_016883426.1:p.Asp106Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant X5 XM_047440281.1:c.248A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform X4 XP_047296237.1:p.Asp83Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant X5 XM_047440281.1:c.248A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform X4 XP_047296237.1:p.Asp83Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant X6 XM_047440282.1:c.245A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform X5 XP_047296238.1:p.Asp82Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant X6 XM_047440282.1:c.245A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform X5 XP_047296238.1:p.Asp82Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant X7 XM_047440283.1:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform X6 XP_047296239.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant X7 XM_047440283.1:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform X6 XP_047296239.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant X8 XM_047440284.1:c.134A>T D [GAT] > V [GTT] Coding Sequence Variant
zinc finger protein 334 isoform X6 XP_047296240.1:p.Asp45Val D (Asp) > V (Val) Missense Variant
ZNF334 transcript variant X8 XM_047440284.1:c.134A>G D [GAT] > G [GGT] Coding Sequence Variant
zinc finger protein 334 isoform X6 XP_047296240.1:p.Asp45Gly D (Asp) > G (Gly) Missense Variant
ZNF334 transcript variant X2 XR_007067464.1:n.1549A>T N/A Non Coding Transcript Variant
ZNF334 transcript variant X2 XR_007067464.1:n.1549A>G N/A Non Coding Transcript 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 T= A C
GRCh38.p14 chr 20 NC_000020.11:g.46503091= NC_000020.11:g.46503091T>A NC_000020.11:g.46503091T>C
GRCh37.p13 chr 20 NC_000020.10:g.45131730= NC_000020.10:g.45131730T>A NC_000020.10:g.45131730T>C
ZNF334 transcript variant 1 NM_018102.6:c.248= NM_018102.6:c.248A>T NM_018102.6:c.248A>G
ZNF334 transcript variant 1 NM_018102.5:c.248= NM_018102.5:c.248A>T NM_018102.5:c.248A>G
ZNF334 transcript variant 1 NM_018102.4:c.248= NM_018102.4:c.248A>T NM_018102.4:c.248A>G
ZNF334 transcript variant 2 NM_199441.3:c.134= NM_199441.3:c.134A>T NM_199441.3:c.134A>G
ZNF334 transcript variant 2 NM_199441.2:c.134= NM_199441.2:c.134A>T NM_199441.2:c.134A>G
ZNF334 transcript variant 2 NM_199441.1:c.134= NM_199441.1:c.134A>T NM_199441.1:c.134A>G
ZNF334 transcript variant 3 NM_001270497.3:c.245= NM_001270497.3:c.245A>T NM_001270497.3:c.245A>G
ZNF334 transcript variant 3 NM_001270497.2:c.245= NM_001270497.2:c.245A>T NM_001270497.2:c.245A>G
ZNF334 transcript variant 3 NM_001270497.1:c.245= NM_001270497.1:c.245A>T NM_001270497.1:c.245A>G
ZNF334 transcript variant X4 XM_017027937.2:c.317= XM_017027937.2:c.317A>T XM_017027937.2:c.317A>G
ZNF334 transcript variant X5 XM_017027937.1:c.317= XM_017027937.1:c.317A>T XM_017027937.1:c.317A>G
ZNF334 transcript variant 10 NM_001353819.2:c.134= NM_001353819.2:c.134A>T NM_001353819.2:c.134A>G
ZNF334 transcript variant 10 NM_001353819.1:c.134= NM_001353819.1:c.134A>T NM_001353819.1:c.134A>G
ZNF334 transcript variant 13 NM_001353822.2:c.245= NM_001353822.2:c.245A>T NM_001353822.2:c.245A>G
ZNF334 transcript variant 13 NM_001353822.1:c.245= NM_001353822.1:c.245A>T NM_001353822.1:c.245A>G
ZNF334 transcript variant 17 NM_001353826.2:c.269= NM_001353826.2:c.269A>T NM_001353826.2:c.269A>G
ZNF334 transcript variant 17 NM_001353826.1:c.269= NM_001353826.1:c.269A>T NM_001353826.1:c.269A>G
ZNF334 transcript variant 14 NM_001353823.2:c.245= NM_001353823.2:c.245A>T NM_001353823.2:c.245A>G
ZNF334 transcript variant 14 NM_001353823.1:c.245= NM_001353823.1:c.245A>T NM_001353823.1:c.245A>G
ZNF334 transcript variant 15 NM_001353824.2:c.248= NM_001353824.2:c.248A>T NM_001353824.2:c.248A>G
ZNF334 transcript variant 15 NM_001353824.1:c.248= NM_001353824.1:c.248A>T NM_001353824.1:c.248A>G
ZNF334 transcript variant 11 NM_001353820.2:c.233= NM_001353820.2:c.233A>T NM_001353820.2:c.233A>G
ZNF334 transcript variant 11 NM_001353820.1:c.233= NM_001353820.1:c.233A>T NM_001353820.1:c.233A>G
ZNF334 transcript variant 5 NM_001353814.2:c.134= NM_001353814.2:c.134A>T NM_001353814.2:c.134A>G
ZNF334 transcript variant 5 NM_001353814.1:c.134= NM_001353814.1:c.134A>T NM_001353814.1:c.134A>G
ZNF334 transcript variant 16 NM_001353825.2:c.317= NM_001353825.2:c.317A>T NM_001353825.2:c.317A>G
ZNF334 transcript variant 16 NM_001353825.1:c.317= NM_001353825.1:c.317A>T NM_001353825.1:c.317A>G
ZNF334 transcript variant 9 NM_001353818.2:c.134= NM_001353818.2:c.134A>T NM_001353818.2:c.134A>G
ZNF334 transcript variant 9 NM_001353818.1:c.134= NM_001353818.1:c.134A>T NM_001353818.1:c.134A>G
ZNF334 transcript variant 12 NM_001353821.2:c.245= NM_001353821.2:c.245A>T NM_001353821.2:c.245A>G
ZNF334 transcript variant 12 NM_001353821.1:c.245= NM_001353821.1:c.245A>T NM_001353821.1:c.245A>G
ZNF334 transcript variant 8 NM_001353817.2:c.134= NM_001353817.2:c.134A>T NM_001353817.2:c.134A>G
ZNF334 transcript variant 8 NM_001353817.1:c.134= NM_001353817.1:c.134A>T NM_001353817.1:c.134A>G
ZNF334 transcript variant 4 NM_001353813.2:c.134= NM_001353813.2:c.134A>T NM_001353813.2:c.134A>G
ZNF334 transcript variant 4 NM_001353813.1:c.134= NM_001353813.1:c.134A>T NM_001353813.1:c.134A>G
ZNF334 transcript variant 6 NM_001353815.2:c.134= NM_001353815.2:c.134A>T NM_001353815.2:c.134A>G
ZNF334 transcript variant 6 NM_001353815.1:c.134= NM_001353815.1:c.134A>T NM_001353815.1:c.134A>G
ZNF334 transcript variant 7 NM_001353816.2:c.134= NM_001353816.2:c.134A>T NM_001353816.2:c.134A>G
ZNF334 transcript variant 7 NM_001353816.1:c.134= NM_001353816.1:c.134A>T NM_001353816.1:c.134A>G
ZNF334 transcript variant X7 XM_047440283.1:c.134= XM_047440283.1:c.134A>T XM_047440283.1:c.134A>G
ZNF334 transcript variant X3 XM_047440280.1:c.269= XM_047440280.1:c.269A>T XM_047440280.1:c.269A>G
ZNF334 transcript variant X1 XM_047440279.1:c.317= XM_047440279.1:c.317A>T XM_047440279.1:c.317A>G
ZNF334 transcript variant X6 XM_047440282.1:c.245= XM_047440282.1:c.245A>T XM_047440282.1:c.245A>G
ZNF334 transcript variant X8 XM_047440284.1:c.134= XM_047440284.1:c.134A>T XM_047440284.1:c.134A>G
ZNF334 transcript variant X2 XR_007067464.1:n.1549= XR_007067464.1:n.1549A>T XR_007067464.1:n.1549A>G
ZNF334 transcript variant 4 NR_073026.1:n.404= NR_073026.1:n.404A>T NR_073026.1:n.404A>G
ZNF334 transcript variant X5 XM_047440281.1:c.248= XM_047440281.1:c.248A>T XM_047440281.1:c.248A>G
zinc finger protein 334 isoform a NP_060572.3:p.Asp83= NP_060572.3:p.Asp83Val NP_060572.3:p.Asp83Gly
zinc finger protein 334 isoform b NP_955473.1:p.Asp45= NP_955473.1:p.Asp45Val NP_955473.1:p.Asp45Gly
zinc finger protein 334 isoform c NP_001257426.1:p.Asp82= NP_001257426.1:p.Asp82Val NP_001257426.1:p.Asp82Gly
zinc finger protein 334 isoform X3 XP_016883426.1:p.Asp106= XP_016883426.1:p.Asp106Val XP_016883426.1:p.Asp106Gly
zinc finger protein 334 isoform b NP_001340748.1:p.Asp45= NP_001340748.1:p.Asp45Val NP_001340748.1:p.Asp45Gly
zinc finger protein 334 isoform c NP_001340751.1:p.Asp82= NP_001340751.1:p.Asp82Val NP_001340751.1:p.Asp82Gly
zinc finger protein 334 isoform f NP_001340755.1:p.Asp90= NP_001340755.1:p.Asp90Val NP_001340755.1:p.Asp90Gly
zinc finger protein 334 isoform c NP_001340752.1:p.Asp82= NP_001340752.1:p.Asp82Val NP_001340752.1:p.Asp82Gly
zinc finger protein 334 isoform a NP_001340753.1:p.Asp83= NP_001340753.1:p.Asp83Val NP_001340753.1:p.Asp83Gly
zinc finger protein 334 isoform d NP_001340749.1:p.Asp78= NP_001340749.1:p.Asp78Val NP_001340749.1:p.Asp78Gly
zinc finger protein 334 isoform b NP_001340743.1:p.Asp45= NP_001340743.1:p.Asp45Val NP_001340743.1:p.Asp45Gly
zinc finger protein 334 isoform e NP_001340754.1:p.Asp106= NP_001340754.1:p.Asp106Val NP_001340754.1:p.Asp106Gly
zinc finger protein 334 isoform b NP_001340747.1:p.Asp45= NP_001340747.1:p.Asp45Val NP_001340747.1:p.Asp45Gly
zinc finger protein 334 isoform c NP_001340750.1:p.Asp82= NP_001340750.1:p.Asp82Val NP_001340750.1:p.Asp82Gly
zinc finger protein 334 isoform b NP_001340746.1:p.Asp45= NP_001340746.1:p.Asp45Val NP_001340746.1:p.Asp45Gly
zinc finger protein 334 isoform b NP_001340742.1:p.Asp45= NP_001340742.1:p.Asp45Val NP_001340742.1:p.Asp45Gly
zinc finger protein 334 isoform b NP_001340744.1:p.Asp45= NP_001340744.1:p.Asp45Val NP_001340744.1:p.Asp45Gly
zinc finger protein 334 isoform b NP_001340745.1:p.Asp45= NP_001340745.1:p.Asp45Val NP_001340745.1:p.Asp45Gly
zinc finger protein 334 isoform X6 XP_047296239.1:p.Asp45= XP_047296239.1:p.Asp45Val XP_047296239.1:p.Asp45Gly
zinc finger protein 334 isoform X2 XP_047296236.1:p.Asp90= XP_047296236.1:p.Asp90Val XP_047296236.1:p.Asp90Gly
zinc finger protein 334 isoform X1 XP_047296235.1:p.Asp106= XP_047296235.1:p.Asp106Val XP_047296235.1:p.Asp106Gly
zinc finger protein 334 isoform X5 XP_047296238.1:p.Asp82= XP_047296238.1:p.Asp82Val XP_047296238.1:p.Asp82Gly
zinc finger protein 334 isoform X6 XP_047296240.1:p.Asp45= XP_047296240.1:p.Asp45Val XP_047296240.1:p.Asp45Gly
zinc finger protein 334 isoform X4 XP_047296237.1:p.Asp83= XP_047296237.1:p.Asp83Val XP_047296237.1:p.Asp83Gly
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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, 2 Frequency submissions
No Submitter Submission ID Date (Build)
1 GNOMAD ss2744650710 Nov 08, 2017 (151)
2 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 13973198 (NC_000020.10:45131729:T:T 231495/231496, NC_000020.10:45131729:T:A 1/231496)
Row 13973199 (NC_000020.10:45131729:T:T 231494/231496, NC_000020.10:45131729:T:C 2/231496)

- Jul 13, 2019 (153)
3 gnomAD - Exomes

Submission ignored due to conflicting rows:
Row 13973198 (NC_000020.10:45131729:T:T 231495/231496, NC_000020.10:45131729:T:A 1/231496)
Row 13973199 (NC_000020.10:45131729:T:T 231494/231496, NC_000020.10:45131729:T:C 2/231496)

- 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
ss2744650710 NC_000020.10:45131729:T:A NC_000020.11:46503090:T:A (self)
ss2744650710 NC_000020.10:45131729:T:C NC_000020.11:46503090:T: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 rs1479981404

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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