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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.

rs1476783615

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chrX:47447844 (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>C
Variation Type
SNV Single Nucleotide Variation
Frequency
C=0.000008 (2/264690, TOPMED)
C=0.00000 (0/14050, ALFA)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
ZNF41 : Synonymous Variant
Publications
0 citations
Genomic View
See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315
Population Group Sample Size Ref Allele Alt Allele Ref HMOZ Alt HMOZ HTRZ HWEP
Total Global 14050 T=1.00000 C=0.00000 1.0 0.0 0.0 N/A
European Sub 9690 T=1.0000 C=0.0000 1.0 0.0 0.0 N/A
African Sub 2898 T=1.0000 C=0.0000 1.0 0.0 0.0 N/A
African Others Sub 114 T=1.000 C=0.000 1.0 0.0 0.0 N/A
African American Sub 2784 T=1.0000 C=0.0000 1.0 0.0 0.0 N/A
Asian Sub 112 T=1.000 C=0.000 1.0 0.0 0.0 N/A
East Asian Sub 86 T=1.00 C=0.00 1.0 0.0 0.0 N/A
Other Asian Sub 26 T=1.00 C=0.00 1.0 0.0 0.0 N/A
Latin American 1 Sub 146 T=1.000 C=0.000 1.0 0.0 0.0 N/A
Latin American 2 Sub 610 T=1.000 C=0.000 1.0 0.0 0.0 N/A
South Asian Sub 98 T=1.00 C=0.00 1.0 0.0 0.0 N/A
Other Sub 496 T=1.000 C=0.000 1.0 0.0 0.0 N/A


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
TopMed Global Study-wide 264690 T=0.999992 C=0.000008
Allele Frequency Aggregator Total Global 14050 T=1.00000 C=0.00000
Allele Frequency Aggregator European Sub 9690 T=1.0000 C=0.0000
Allele Frequency Aggregator African Sub 2898 T=1.0000 C=0.0000
Allele Frequency Aggregator Latin American 2 Sub 610 T=1.000 C=0.000
Allele Frequency Aggregator Other Sub 496 T=1.000 C=0.000
Allele Frequency Aggregator Latin American 1 Sub 146 T=1.000 C=0.000
Allele Frequency Aggregator Asian Sub 112 T=1.000 C=0.000
Allele Frequency Aggregator South Asian Sub 98 T=1.00 C=0.00
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 X NC_000023.11:g.47447844T>C
GRCh37.p13 chr X NC_000023.10:g.47307243T>C
ZNF41 RefSeqGene NG_008238.1:g.40103A>G
Gene: ZNF41, zinc finger protein 41 (minus strand)
Molecule type Change Amino acid[Codon] SO Term
ZNF41 transcript variant 17 NM_001324154.1:c.2028A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform e NP_001311083.1:p.Lys676= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 2 NM_153380.3:c.1926A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform a NP_700359.1:p.Lys642= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 19 NM_001324156.1:c.1824A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform g NP_001311085.1:p.Lys608= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 20 NM_001324157.1:c.1818A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform h NP_001311086.1:p.Lys606= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 18 NM_001324155.1:c.2052A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform f NP_001311084.1:p.Lys684= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 6 NM_001324142.2:c.1932A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform c NP_001311071.1:p.Lys644= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 13 NM_001324150.2:c.1926A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform a NP_001311079.1:p.Lys642= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 10 NM_001324147.2:c.1926A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform a NP_001311076.1:p.Lys642= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 16 NM_001324153.2:c.1956A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform d NP_001311082.1:p.Lys652= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 1 NM_007130.4:c.1926A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform a NP_009061.1:p.Lys642= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 5 NM_001324141.2:c.1668A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform b NP_001311070.1:p.Lys556= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 7 NM_001324143.2:c.1668A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform b NP_001311072.1:p.Lys556= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 3 NM_001324139.2:c.1668A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform b NP_001311068.1:p.Lys556= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 8 NM_001324144.2:c.1926A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform a NP_001311073.1:p.Lys642= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 15 NM_001324152.2:c.1668A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform b NP_001311081.1:p.Lys556= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 14 NM_001324151.2:c.1956A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform d NP_001311080.1:p.Lys652= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 9 NM_001324145.2:c.1668A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform b NP_001311074.1:p.Lys556= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 4 NM_001324140.2:c.1926A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform a NP_001311069.1:p.Lys642= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 11 NM_001324148.2:c.1932A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform c NP_001311077.1:p.Lys644= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant 12 NM_001324149.2:c.1668A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform b NP_001311078.1:p.Lys556= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X1 XM_006724550.4:c.2028A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X1 XP_006724613.1:p.Lys676= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X2 XM_017029812.2:c.2028A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X1 XP_016885301.1:p.Lys676= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X3 XM_017029811.3:c.2028A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X1 XP_016885300.1:p.Lys676= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X4 XM_017029814.3:c.2028A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X1 XP_016885303.1:p.Lys676= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X5 XM_017029810.3:c.2028A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X1 XP_016885299.1:p.Lys676= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X6 XM_017029813.2:c.2028A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X1 XP_016885302.1:p.Lys676= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X7 XM_017029815.2:c.2028A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X1 XP_016885304.1:p.Lys676= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X8 XM_047442471.1:c.2028A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X1 XP_047298427.1:p.Lys676= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X9 XM_006724555.4:c.1956A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X2 XP_006724618.1:p.Lys652= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X10 XM_047442472.1:c.1956A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X2 XP_047298428.1:p.Lys652= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X11 XM_047442473.1:c.1956A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X2 XP_047298429.1:p.Lys652= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X12 XM_047442474.1:c.1956A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X2 XP_047298430.1:p.Lys652= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X13 XM_017029816.2:c.1956A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X2 XP_016885305.1:p.Lys652= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X14 XM_047442475.1:c.1932A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X3 XP_047298431.1:p.Lys644= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X15 XM_047442476.1:c.1932A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X3 XP_047298432.1:p.Lys644= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X16 XM_047442477.1:c.1932A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X3 XP_047298433.1:p.Lys644= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X17 XM_047442478.1:c.1932A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X3 XP_047298434.1:p.Lys644= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X18 XM_047442479.1:c.1932A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X3 XP_047298435.1:p.Lys644= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X19 XM_047442480.1:c.1932A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X3 XP_047298436.1:p.Lys644= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X20 XM_047442481.1:c.1926A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X4 XP_047298437.1:p.Lys642= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X21 XM_047442482.1:c.1926A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X4 XP_047298438.1:p.Lys642= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X22 XM_017029817.2:c.1926A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X4 XP_016885306.1:p.Lys642= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X23 XM_047442483.1:c.1668A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X5 XP_047298439.1:p.Lys556= K (Lys) > K (Lys) Synonymous Variant
ZNF41 transcript variant X24 XM_047442484.1:c.1668A>G K [AAA] > K [AAG] Coding Sequence Variant
zinc finger protein 41 isoform X5 XP_047298440.1:p.Lys556= K (Lys) > K (Lys) Synonymous 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= C
GRCh38.p14 chr X NC_000023.11:g.47447844= NC_000023.11:g.47447844T>C
GRCh37.p13 chr X NC_000023.10:g.47307243= NC_000023.10:g.47307243T>C
ZNF41 RefSeqGene NG_008238.1:g.40103= NG_008238.1:g.40103A>G
ZNF41 transcript variant 1 NM_007130.4:c.1926= NM_007130.4:c.1926A>G
ZNF41 transcript variant 1 NM_007130.3:c.1926= NM_007130.3:c.1926A>G
ZNF41 transcript variant 1 NM_007130.2:c.1926= NM_007130.2:c.1926A>G
ZNF41 transcript variant 2 NM_153380.3:c.1926= NM_153380.3:c.1926A>G
ZNF41 transcript variant 2 NM_153380.2:c.1926= NM_153380.2:c.1926A>G
ZNF41 transcript variant 13 NM_001324150.2:c.1926= NM_001324150.2:c.1926A>G
ZNF41 transcript variant 13 NM_001324150.1:c.1926= NM_001324150.1:c.1926A>G
ZNF41 transcript variant 15 NM_001324152.2:c.1668= NM_001324152.2:c.1668A>G
ZNF41 transcript variant 15 NM_001324152.1:c.1668= NM_001324152.1:c.1668A>G
ZNF41 transcript variant 14 NM_001324151.2:c.1956= NM_001324151.2:c.1956A>G
ZNF41 transcript variant 14 NM_001324151.1:c.1956= NM_001324151.1:c.1956A>G
ZNF41 transcript variant 11 NM_001324148.2:c.1932= NM_001324148.2:c.1932A>G
ZNF41 transcript variant 11 NM_001324148.1:c.1932= NM_001324148.1:c.1932A>G
ZNF41 transcript variant 8 NM_001324144.2:c.1926= NM_001324144.2:c.1926A>G
ZNF41 transcript variant 8 NM_001324144.1:c.1926= NM_001324144.1:c.1926A>G
ZNF41 transcript variant 10 NM_001324147.2:c.1926= NM_001324147.2:c.1926A>G
ZNF41 transcript variant 10 NM_001324147.1:c.1926= NM_001324147.1:c.1926A>G
ZNF41 transcript variant 16 NM_001324153.2:c.1956= NM_001324153.2:c.1956A>G
ZNF41 transcript variant 16 NM_001324153.1:c.1956= NM_001324153.1:c.1956A>G
ZNF41 transcript variant 6 NM_001324142.2:c.1932= NM_001324142.2:c.1932A>G
ZNF41 transcript variant 6 NM_001324142.1:c.1932= NM_001324142.1:c.1932A>G
ZNF41 transcript variant 4 NM_001324140.2:c.1926= NM_001324140.2:c.1926A>G
ZNF41 transcript variant 4 NM_001324140.1:c.1926= NM_001324140.1:c.1926A>G
ZNF41 transcript variant 12 NM_001324149.2:c.1668= NM_001324149.2:c.1668A>G
ZNF41 transcript variant 12 NM_001324149.1:c.1668= NM_001324149.1:c.1668A>G
ZNF41 transcript variant 7 NM_001324143.2:c.1668= NM_001324143.2:c.1668A>G
ZNF41 transcript variant 7 NM_001324143.1:c.1668= NM_001324143.1:c.1668A>G
ZNF41 transcript variant 9 NM_001324145.2:c.1668= NM_001324145.2:c.1668A>G
ZNF41 transcript variant 9 NM_001324145.1:c.1668= NM_001324145.1:c.1668A>G
ZNF41 transcript variant 5 NM_001324141.2:c.1668= NM_001324141.2:c.1668A>G
ZNF41 transcript variant 5 NM_001324141.1:c.1668= NM_001324141.1:c.1668A>G
ZNF41 transcript variant 3 NM_001324139.2:c.1668= NM_001324139.2:c.1668A>G
ZNF41 transcript variant 3 NM_001324139.1:c.1668= NM_001324139.1:c.1668A>G
ZNF41 transcript variant 18 NM_001324155.1:c.2052= NM_001324155.1:c.2052A>G
ZNF41 transcript variant 17 NM_001324154.1:c.2028= NM_001324154.1:c.2028A>G
ZNF41 transcript variant 19 NM_001324156.1:c.1824= NM_001324156.1:c.1824A>G
ZNF41 transcript variant 20 NM_001324157.1:c.1818= NM_001324157.1:c.1818A>G
ZNF41 transcript variant X1 XM_006724550.4:c.2028= XM_006724550.4:c.2028A>G
ZNF41 transcript variant X1 XM_006724550.3:c.2028= XM_006724550.3:c.2028A>G
ZNF41 transcript variant X4 XM_006724550.2:c.2028= XM_006724550.2:c.2028A>G
ZNF41 transcript variant X7 XM_006724550.1:c.2028= XM_006724550.1:c.2028A>G
ZNF41 transcript variant X9 XM_006724555.4:c.1956= XM_006724555.4:c.1956A>G
ZNF41 transcript variant X8 XM_006724555.3:c.1956= XM_006724555.3:c.1956A>G
ZNF41 transcript variant X6 XM_006724555.2:c.1956= XM_006724555.2:c.1956A>G
ZNF41 transcript variant X12 XM_006724555.1:c.1956= XM_006724555.1:c.1956A>G
ZNF41 transcript variant X3 XM_017029811.3:c.2028= XM_017029811.3:c.2028A>G
ZNF41 transcript variant X3 XM_017029811.2:c.2028= XM_017029811.2:c.2028A>G
ZNF41 transcript variant X3 XM_017029811.1:c.2028= XM_017029811.1:c.2028A>G
ZNF41 transcript variant X5 XM_017029810.3:c.2028= XM_017029810.3:c.2028A>G
ZNF41 transcript variant X2 XM_017029810.2:c.2028= XM_017029810.2:c.2028A>G
ZNF41 transcript variant X2 XM_017029810.1:c.2028= XM_017029810.1:c.2028A>G
ZNF41 transcript variant X4 XM_017029814.3:c.2028= XM_017029814.3:c.2028A>G
ZNF41 transcript variant X6 XM_017029814.2:c.2028= XM_017029814.2:c.2028A>G
ZNF41 transcript variant X6 XM_017029814.1:c.2028= XM_017029814.1:c.2028A>G
ZNF41 transcript variant X2 XM_017029812.2:c.2028= XM_017029812.2:c.2028A>G
ZNF41 transcript variant X4 XM_017029812.1:c.2028= XM_017029812.1:c.2028A>G
ZNF41 transcript variant X6 XM_017029813.2:c.2028= XM_017029813.2:c.2028A>G
ZNF41 transcript variant X5 XM_017029813.1:c.2028= XM_017029813.1:c.2028A>G
ZNF41 transcript variant X7 XM_017029815.2:c.2028= XM_017029815.2:c.2028A>G
ZNF41 transcript variant X7 XM_017029815.1:c.2028= XM_017029815.1:c.2028A>G
ZNF41 transcript variant X13 XM_017029816.2:c.1956= XM_017029816.2:c.1956A>G
ZNF41 transcript variant X9 XM_017029816.1:c.1956= XM_017029816.1:c.1956A>G
ZNF41 transcript variant X22 XM_017029817.2:c.1926= XM_017029817.2:c.1926A>G
ZNF41 transcript variant X10 XM_017029817.1:c.1926= XM_017029817.1:c.1926A>G
ZNF41 transcript variant X14 XM_047442475.1:c.1932= XM_047442475.1:c.1932A>G
ZNF41 transcript variant X10 XM_047442472.1:c.1956= XM_047442472.1:c.1956A>G
ZNF41 transcript variant X12 XM_047442474.1:c.1956= XM_047442474.1:c.1956A>G
ZNF41 transcript variant X15 XM_047442476.1:c.1932= XM_047442476.1:c.1932A>G
ZNF41 transcript variant X18 XM_047442479.1:c.1932= XM_047442479.1:c.1932A>G
ZNF41 transcript variant X8 XM_047442471.1:c.2028= XM_047442471.1:c.2028A>G
ZNF41 transcript variant X11 XM_047442473.1:c.1956= XM_047442473.1:c.1956A>G
ZNF41 transcript variant X16 XM_047442477.1:c.1932= XM_047442477.1:c.1932A>G
ZNF41 transcript variant X20 XM_047442481.1:c.1926= XM_047442481.1:c.1926A>G
ZNF41 transcript variant X17 XM_047442478.1:c.1932= XM_047442478.1:c.1932A>G
ZNF41 transcript variant X19 XM_047442480.1:c.1932= XM_047442480.1:c.1932A>G
ZNF41 transcript variant X21 XM_047442482.1:c.1926= XM_047442482.1:c.1926A>G
ZNF41 transcript variant X23 XM_047442483.1:c.1668= XM_047442483.1:c.1668A>G
ZNF41 transcript variant X24 XM_047442484.1:c.1668= XM_047442484.1:c.1668A>G
zinc finger protein 41 isoform a NP_009061.1:p.Lys642= NP_009061.1:p.Lys642=
zinc finger protein 41 isoform a NP_700359.1:p.Lys642= NP_700359.1:p.Lys642=
zinc finger protein 41 isoform a NP_001311079.1:p.Lys642= NP_001311079.1:p.Lys642=
zinc finger protein 41 isoform b NP_001311081.1:p.Lys556= NP_001311081.1:p.Lys556=
zinc finger protein 41 isoform d NP_001311080.1:p.Lys652= NP_001311080.1:p.Lys652=
zinc finger protein 41 isoform c NP_001311077.1:p.Lys644= NP_001311077.1:p.Lys644=
zinc finger protein 41 isoform a NP_001311073.1:p.Lys642= NP_001311073.1:p.Lys642=
zinc finger protein 41 isoform a NP_001311076.1:p.Lys642= NP_001311076.1:p.Lys642=
zinc finger protein 41 isoform d NP_001311082.1:p.Lys652= NP_001311082.1:p.Lys652=
zinc finger protein 41 isoform c NP_001311071.1:p.Lys644= NP_001311071.1:p.Lys644=
zinc finger protein 41 isoform a NP_001311069.1:p.Lys642= NP_001311069.1:p.Lys642=
zinc finger protein 41 isoform b NP_001311078.1:p.Lys556= NP_001311078.1:p.Lys556=
zinc finger protein 41 isoform b NP_001311072.1:p.Lys556= NP_001311072.1:p.Lys556=
zinc finger protein 41 isoform b NP_001311074.1:p.Lys556= NP_001311074.1:p.Lys556=
zinc finger protein 41 isoform b NP_001311070.1:p.Lys556= NP_001311070.1:p.Lys556=
zinc finger protein 41 isoform b NP_001311068.1:p.Lys556= NP_001311068.1:p.Lys556=
zinc finger protein 41 isoform f NP_001311084.1:p.Lys684= NP_001311084.1:p.Lys684=
zinc finger protein 41 isoform e NP_001311083.1:p.Lys676= NP_001311083.1:p.Lys676=
zinc finger protein 41 isoform g NP_001311085.1:p.Lys608= NP_001311085.1:p.Lys608=
zinc finger protein 41 isoform h NP_001311086.1:p.Lys606= NP_001311086.1:p.Lys606=
zinc finger protein 41 isoform X1 XP_006724613.1:p.Lys676= XP_006724613.1:p.Lys676=
zinc finger protein 41 isoform X2 XP_006724618.1:p.Lys652= XP_006724618.1:p.Lys652=
zinc finger protein 41 isoform X1 XP_016885300.1:p.Lys676= XP_016885300.1:p.Lys676=
zinc finger protein 41 isoform X1 XP_016885299.1:p.Lys676= XP_016885299.1:p.Lys676=
zinc finger protein 41 isoform X1 XP_016885303.1:p.Lys676= XP_016885303.1:p.Lys676=
zinc finger protein 41 isoform X1 XP_016885301.1:p.Lys676= XP_016885301.1:p.Lys676=
zinc finger protein 41 isoform X1 XP_016885302.1:p.Lys676= XP_016885302.1:p.Lys676=
zinc finger protein 41 isoform X1 XP_016885304.1:p.Lys676= XP_016885304.1:p.Lys676=
zinc finger protein 41 isoform X2 XP_016885305.1:p.Lys652= XP_016885305.1:p.Lys652=
zinc finger protein 41 isoform X4 XP_016885306.1:p.Lys642= XP_016885306.1:p.Lys642=
zinc finger protein 41 isoform X3 XP_047298431.1:p.Lys644= XP_047298431.1:p.Lys644=
zinc finger protein 41 isoform X2 XP_047298428.1:p.Lys652= XP_047298428.1:p.Lys652=
zinc finger protein 41 isoform X2 XP_047298430.1:p.Lys652= XP_047298430.1:p.Lys652=
zinc finger protein 41 isoform X3 XP_047298432.1:p.Lys644= XP_047298432.1:p.Lys644=
zinc finger protein 41 isoform X3 XP_047298435.1:p.Lys644= XP_047298435.1:p.Lys644=
zinc finger protein 41 isoform X1 XP_047298427.1:p.Lys676= XP_047298427.1:p.Lys676=
zinc finger protein 41 isoform X2 XP_047298429.1:p.Lys652= XP_047298429.1:p.Lys652=
zinc finger protein 41 isoform X3 XP_047298433.1:p.Lys644= XP_047298433.1:p.Lys644=
zinc finger protein 41 isoform X4 XP_047298437.1:p.Lys642= XP_047298437.1:p.Lys642=
zinc finger protein 41 isoform X3 XP_047298434.1:p.Lys644= XP_047298434.1:p.Lys644=
zinc finger protein 41 isoform X3 XP_047298436.1:p.Lys644= XP_047298436.1:p.Lys644=
zinc finger protein 41 isoform X4 XP_047298438.1:p.Lys642= XP_047298438.1:p.Lys642=
zinc finger protein 41 isoform X5 XP_047298439.1:p.Lys556= XP_047298439.1:p.Lys556=
zinc finger protein 41 isoform X5 XP_047298440.1:p.Lys556= XP_047298440.1:p.Lys556=
Help

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 TOPMED ss5121981877 Apr 27, 2021 (155)
2 TopMed NC_000023.11 - 47447844 Apr 27, 2021 (155)
3 ALFA NC_000023.11 - 47447844 Apr 27, 2021 (155)
Help

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
685588234, 1003252732, ss5121981877 NC_000023.11:47447843:T:C NC_000023.11:47447843: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 rs1476783615

Help

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
Top▲ Help

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