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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.

rs1474835561

Current Build 156

Released September 21, 2022

Organism
Homo sapiens
Position
chrY:13369298 (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=0.00002 (1/45390, GnomAD_exome)
Clinical Significance
Not Reported in ClinVar
Gene : Consequence
UTY : 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 45390 T=0.99998 C=0.00002
gnomAD - Exomes European Sub 25069 T=0.99996 C=0.00004
gnomAD - Exomes Asian Sub 10669 T=1.00000 C=0.00000
gnomAD - Exomes American Sub 4514 T=1.0000 C=0.0000
gnomAD - Exomes Ashkenazi Jewish Sub 2152 T=1.0000 C=0.0000
gnomAD - Exomes African Sub 1894 T=1.0000 C=0.0000
gnomAD - Exomes Other Sub 1092 T=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 Y NC_000024.10:g.13369298T>C
GRCh37.p13 chr Y NC_000024.9:g.15481178T>C
Gene: UTY, ubiquitously transcribed tetratricopeptide repeat containing, Y-linked (minus strand)
Molecule type Change Amino acid[Codon] SO Term
UTY transcript variant 2 NM_182659.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 2 NP_872600.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 1 NM_182660.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 1 NP_872601.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 3 NM_007125.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 3 NP_009056.3:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 5 NM_001258250.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 5 NP_001245179.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 6 NM_001258251.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 6 NP_001245180.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 7 NM_001258252.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 7 NP_001245181.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 8 NM_001258253.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 8 NP_001245182.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 9 NM_001258254.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 9 NP_001245183.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 10 NM_001258255.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 10 NP_001245184.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 11 NM_001258256.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 11 NP_001245185.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 12 NM_001258257.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 12 NP_001245186.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 13 NM_001258258.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 13 NP_001245187.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 14 NM_001258259.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 14 NP_001245188.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 15 NM_001258260.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 15 NP_001245189.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 16 NM_001258261.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 16 NP_001245190.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 17 NM_001258262.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 17 NP_001245191.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 18 NM_001258263.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 18 NP_001245192.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 19 NM_001258264.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 19 NP_001245193.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 20 NM_001258265.1:c.448A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 20 NP_001245194.1:p.Asn150Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 21 NM_001258266.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 21 NP_001245195.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 22 NM_001258267.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 22 NP_001245196.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 23 NM_001258268.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 23 NP_001245197.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 24 NM_001258269.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 24 NP_001245198.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 25 NM_001258270.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 25 NP_001245199.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 4 NM_001258249.2:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 4 NP_001245178.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 85 NM_001400183.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 33 NP_001387112.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 87 NM_001400187.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 35 NP_001387116.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 88 NM_001400189.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 36 NP_001387118.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 84 NM_001400181.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 32 NP_001387110.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 91 NM_001400199.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 39 NP_001387128.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 79 NM_001400171.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 27 NP_001387100.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 83 NM_001400178.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 31 NP_001387107.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 86 NM_001400185.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 34 NP_001387114.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 80 NM_001400173.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 28 NP_001387102.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 90 NM_001400195.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 38 NP_001387124.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 81 NM_001400175.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 29 NP_001387104.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 82 NM_001400177.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 30 NP_001387106.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 78 NM_001400170.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 26 NP_001387099.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 89 NM_001400192.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform 37 NP_001387121.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant 26 NR_047596.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 27 NR_047597.1:n.1808A>G N/A Non Coding Transcript Variant
UTY transcript variant 28 NR_047598.1:n.1808A>G N/A Non Coding Transcript Variant
UTY transcript variant 29 NR_047599.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 30 NR_047600.1:n.1667A>G N/A Non Coding Transcript Variant
UTY transcript variant 31 NR_047601.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 32 NR_047602.1:n.1667A>G N/A Non Coding Transcript Variant
UTY transcript variant 33 NR_047603.1:n.1825A>G N/A Non Coding Transcript Variant
UTY transcript variant 34 NR_047604.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 35 NR_047605.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 36 NR_047606.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 37 NR_047607.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 38 NR_047608.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 39 NR_047609.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 40 NR_047610.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 41 NR_047611.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 42 NR_047612.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 43 NR_047613.1:n.1652A>G N/A Non Coding Transcript Variant
UTY transcript variant 44 NR_047614.1:n.1816A>G N/A Non Coding Transcript Variant
UTY transcript variant 45 NR_047615.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 46 NR_047616.1:n.1816A>G N/A Non Coding Transcript Variant
UTY transcript variant 47 NR_047617.1:n.1808A>G N/A Non Coding Transcript Variant
UTY transcript variant 48 NR_047618.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 49 NR_047619.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 50 NR_047620.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 51 NR_047621.1:n.1773A>G N/A Non Coding Transcript Variant
UTY transcript variant 52 NR_047622.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 53 NR_047623.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 54 NR_047624.1:n.1922A>G N/A Non Coding Transcript Variant
UTY transcript variant 55 NR_047625.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 56 NR_047626.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 57 NR_047627.1:n.1667A>G N/A Non Coding Transcript Variant
UTY transcript variant 58 NR_047628.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 59 NR_047629.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 61 NR_047631.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 60 NR_047630.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 62 NR_047632.1:n.1782A>G N/A Non Coding Transcript Variant
UTY transcript variant 64 NR_047634.1:n.1667A>G N/A Non Coding Transcript Variant
UTY transcript variant 63 NR_047633.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 65 NR_047635.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 66 NR_047636.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 67 NR_047637.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 68 NR_047638.1:n.1773A>G N/A Non Coding Transcript Variant
UTY transcript variant 70 NR_047640.1:n.1808A>G N/A Non Coding Transcript Variant
UTY transcript variant 71 NR_047641.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 72 NR_047642.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 73 NR_047643.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 74 NR_047644.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 75 NR_047645.1:n.1773A>G N/A Non Coding Transcript Variant
UTY transcript variant 76 NR_047646.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 77 NR_047647.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant 93 NR_174405.1:n.1065A>G N/A Non Coding Transcript Variant
UTY transcript variant 92 NR_174404.1:n.1065A>G N/A Non Coding Transcript Variant
UTY transcript variant 69 NR_047639.1:n. N/A Intron Variant
UTY transcript variant X1 XM_011531441.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X1 XP_011529743.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X2 XM_011531442.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X2 XP_011529744.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X3 XM_011531443.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X3 XP_011529745.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X4 XM_047442746.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X4 XP_047298702.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X5 XM_011531445.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X5 XP_011529747.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X6 XM_011531446.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X6 XP_011529748.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X7 XM_011531447.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X7 XP_011529749.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X8 XM_011531448.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X8 XP_011529750.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X9 XM_011531451.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X9 XP_011529753.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X10 XM_011531453.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X10 XP_011529755.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X11 XM_011531454.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X11 XP_011529756.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X12 XM_011531455.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X12 XP_011529757.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X13 XM_047442747.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X13 XP_047298703.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X14 XM_047442748.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X14 XP_047298704.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X15 XM_047442749.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X15 XP_047298705.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X16 XM_047442750.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X16 XP_047298706.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X17 XM_047442751.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X17 XP_047298707.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X18 XM_047442752.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X18 XP_047298708.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X19 XM_047442753.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X19 XP_047298709.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X20 XM_047442754.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X20 XP_047298710.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X21 XM_011531459.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X21 XP_011529761.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X22 XM_047442755.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X22 XP_047298711.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X24 XM_017030070.3:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X23 XP_016885559.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X26 XM_011531460.4:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X24 XP_011529762.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X27 XM_047442756.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X25 XP_047298712.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X28 XM_047442757.1:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X26 XP_047298713.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X29 XM_017030071.3:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X27 XP_016885560.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X30 XM_017030073.3:c.697A>G N [AAC] > D [GAC] Coding Sequence Variant
histone demethylase UTY isoform X28 XP_016885562.1:p.Asn233Asp N (Asn) > D (Asp) Missense Variant
UTY transcript variant X23 XR_007068451.1:n.1702A>G N/A Non Coding Transcript Variant
UTY transcript variant X25 XR_007068452.1:n.1702A>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
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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 Y NC_000024.10:g.13369298= NC_000024.10:g.13369298T>C
GRCh37.p13 chr Y NC_000024.9:g.15481178= NC_000024.9:g.15481178T>C
UTY transcript variant X12 XM_011531455.4:c.697= XM_011531455.4:c.697A>G
UTY transcript variant X14 XM_011531455.3:c.697= XM_011531455.3:c.697A>G
UTY transcript variant X14 XM_011531455.2:c.697= XM_011531455.2:c.697A>G
UTY transcript variant X15 XM_011531455.1:c.697= XM_011531455.1:c.697A>G
UTY transcript variant X10 XM_011531453.4:c.697= XM_011531453.4:c.697A>G
UTY transcript variant X12 XM_011531453.3:c.697= XM_011531453.3:c.697A>G
UTY transcript variant X12 XM_011531453.2:c.697= XM_011531453.2:c.697A>G
UTY transcript variant X13 XM_011531453.1:c.697= XM_011531453.1:c.697A>G
UTY transcript variant X11 XM_011531454.4:c.697= XM_011531454.4:c.697A>G
UTY transcript variant X13 XM_011531454.3:c.697= XM_011531454.3:c.697A>G
UTY transcript variant X13 XM_011531454.2:c.697= XM_011531454.2:c.697A>G
UTY transcript variant X14 XM_011531454.1:c.697= XM_011531454.1:c.697A>G
UTY transcript variant 3 NM_007125.4:c.697= NM_007125.4:c.697A>G
UTY transcript variant X1 XM_011531441.4:c.697= XM_011531441.4:c.697A>G
UTY transcript variant X1 XM_011531441.3:c.697= XM_011531441.3:c.697A>G
UTY transcript variant X1 XM_011531441.2:c.697= XM_011531441.2:c.697A>G
UTY transcript variant X1 XM_011531441.1:c.697= XM_011531441.1:c.697A>G
UTY transcript variant X2 XM_011531442.4:c.697= XM_011531442.4:c.697A>G
UTY transcript variant X2 XM_011531442.3:c.697= XM_011531442.3:c.697A>G
UTY transcript variant X2 XM_011531442.2:c.697= XM_011531442.2:c.697A>G
UTY transcript variant X2 XM_011531442.1:c.697= XM_011531442.1:c.697A>G
UTY transcript variant X3 XM_011531443.4:c.697= XM_011531443.4:c.697A>G
UTY transcript variant X3 XM_011531443.3:c.697= XM_011531443.3:c.697A>G
UTY transcript variant X3 XM_011531443.2:c.697= XM_011531443.2:c.697A>G
UTY transcript variant X3 XM_011531443.1:c.697= XM_011531443.1:c.697A>G
UTY transcript variant X5 XM_011531445.4:c.697= XM_011531445.4:c.697A>G
UTY transcript variant X4 XM_011531445.3:c.697= XM_011531445.3:c.697A>G
UTY transcript variant X4 XM_011531445.2:c.697= XM_011531445.2:c.697A>G
UTY transcript variant X5 XM_011531445.1:c.697= XM_011531445.1:c.697A>G
UTY transcript variant X6 XM_011531446.4:c.697= XM_011531446.4:c.697A>G
UTY transcript variant X5 XM_011531446.3:c.697= XM_011531446.3:c.697A>G
UTY transcript variant X5 XM_011531446.2:c.697= XM_011531446.2:c.697A>G
UTY transcript variant X6 XM_011531446.1:c.697= XM_011531446.1:c.697A>G
UTY transcript variant X7 XM_011531447.4:c.697= XM_011531447.4:c.697A>G
UTY transcript variant X6 XM_011531447.3:c.697= XM_011531447.3:c.697A>G
UTY transcript variant X6 XM_011531447.2:c.697= XM_011531447.2:c.697A>G
UTY transcript variant X7 XM_011531447.1:c.697= XM_011531447.1:c.697A>G
UTY transcript variant X8 XM_011531448.4:c.697= XM_011531448.4:c.697A>G
UTY transcript variant X7 XM_011531448.3:c.697= XM_011531448.3:c.697A>G
UTY transcript variant X7 XM_011531448.2:c.697= XM_011531448.2:c.697A>G
UTY transcript variant X8 XM_011531448.1:c.697= XM_011531448.1:c.697A>G
UTY transcript variant X9 XM_011531451.4:c.697= XM_011531451.4:c.697A>G
UTY transcript variant X10 XM_011531451.3:c.697= XM_011531451.3:c.697A>G
UTY transcript variant X10 XM_011531451.2:c.697= XM_011531451.2:c.697A>G
UTY transcript variant X11 XM_011531451.1:c.697= XM_011531451.1:c.697A>G
UTY transcript variant X21 XM_011531459.4:c.697= XM_011531459.4:c.697A>G
UTY transcript variant X18 XM_011531459.3:c.697= XM_011531459.3:c.697A>G
UTY transcript variant X19 XM_011531459.2:c.697= XM_011531459.2:c.697A>G
UTY transcript variant X19 XM_011531459.1:c.697= XM_011531459.1:c.697A>G
UTY transcript variant X26 XM_011531460.4:c.697= XM_011531460.4:c.697A>G
UTY transcript variant X23 XM_011531460.3:c.697= XM_011531460.3:c.697A>G
UTY transcript variant X25 XM_011531460.2:c.697= XM_011531460.2:c.697A>G
UTY transcript variant X21 XM_011531460.1:c.697= XM_011531460.1:c.697A>G
UTY transcript variant X24 XM_017030070.3:c.697= XM_017030070.3:c.697A>G
UTY transcript variant X21 XM_017030070.2:c.697= XM_017030070.2:c.697A>G
UTY transcript variant X23 XM_017030070.1:c.697= XM_017030070.1:c.697A>G
UTY transcript variant X29 XM_017030071.3:c.697= XM_017030071.3:c.697A>G
UTY transcript variant X26 XM_017030071.2:c.697= XM_017030071.2:c.697A>G
UTY transcript variant X28 XM_017030071.1:c.697= XM_017030071.1:c.697A>G
UTY transcript variant X30 XM_017030073.3:c.697= XM_017030073.3:c.697A>G
UTY transcript variant X34 XM_017030073.2:c.697= XM_017030073.2:c.697A>G
UTY transcript variant X35 XM_017030073.1:c.697= XM_017030073.1:c.697A>G
UTY transcript variant 4 NM_001258249.2:c.697= NM_001258249.2:c.697A>G
UTY transcript variant 4 NM_001258249.1:c.697= NM_001258249.1:c.697A>G
UTY transcript variant X14 XM_047442748.1:c.697= XM_047442748.1:c.697A>G
UTY transcript variant X15 XM_047442749.1:c.697= XM_047442749.1:c.697A>G
UTY transcript variant X17 XM_047442751.1:c.697= XM_047442751.1:c.697A>G
UTY transcript variant X18 XM_047442752.1:c.697= XM_047442752.1:c.697A>G
UTY transcript variant X20 XM_047442754.1:c.697= XM_047442754.1:c.697A>G
UTY transcript variant 37 NR_047607.1:n.1702= NR_047607.1:n.1702A>G
UTY transcript variant 28 NR_047598.1:n.1808= NR_047598.1:n.1808A>G
UTY transcript variant 54 NR_047624.1:n.1922= NR_047624.1:n.1922A>G
UTY transcript variant X13 XM_047442747.1:c.697= XM_047442747.1:c.697A>G
UTY transcript variant 75 NR_047645.1:n.1773= NR_047645.1:n.1773A>G
UTY transcript variant X16 XM_047442750.1:c.697= XM_047442750.1:c.697A>G
UTY transcript variant 74 NR_047644.1:n.1702= NR_047644.1:n.1702A>G
UTY transcript variant 13 NM_001258258.1:c.697= NM_001258258.1:c.697A>G
UTY transcript variant 29 NR_047599.1:n.1702= NR_047599.1:n.1702A>G
UTY transcript variant 7 NM_001258252.1:c.697= NM_001258252.1:c.697A>G
UTY transcript variant 16 NM_001258261.1:c.697= NM_001258261.1:c.697A>G
UTY transcript variant 33 NR_047603.1:n.1825= NR_047603.1:n.1825A>G
UTY transcript variant 27 NR_047597.1:n.1808= NR_047597.1:n.1808A>G
UTY transcript variant 72 NR_047642.1:n.1702= NR_047642.1:n.1702A>G
UTY transcript variant 48 NR_047618.1:n.1702= NR_047618.1:n.1702A>G
UTY transcript variant 15 NM_001258260.1:c.697= NM_001258260.1:c.697A>G
UTY transcript variant 19 NM_001258264.1:c.697= NM_001258264.1:c.697A>G
UTY transcript variant 67 NR_047637.1:n.1702= NR_047637.1:n.1702A>G
UTY transcript variant 71 NR_047641.1:n.1702= NR_047641.1:n.1702A>G
UTY transcript variant 21 NM_001258266.1:c.697= NM_001258266.1:c.697A>G
UTY transcript variant X19 XM_047442753.1:c.697= XM_047442753.1:c.697A>G
UTY transcript variant 6 NM_001258251.1:c.697= NM_001258251.1:c.697A>G
UTY transcript variant 22 NM_001258267.1:c.697= NM_001258267.1:c.697A>G
UTY transcript variant 32 NR_047602.1:n.1667= NR_047602.1:n.1667A>G
UTY transcript variant 11 NM_001258256.1:c.697= NM_001258256.1:c.697A>G
UTY transcript variant 77 NR_047647.1:n.1702= NR_047647.1:n.1702A>G
UTY transcript variant 14 NM_001258259.1:c.697= NM_001258259.1:c.697A>G
UTY transcript variant 30 NR_047600.1:n.1667= NR_047600.1:n.1667A>G
UTY transcript variant 17 NM_001258262.1:c.697= NM_001258262.1:c.697A>G
UTY transcript variant 68 NR_047638.1:n.1773= NR_047638.1:n.1773A>G
UTY transcript variant 8 NM_001258253.1:c.697= NM_001258253.1:c.697A>G
UTY transcript variant 76 NR_047646.1:n.1702= NR_047646.1:n.1702A>G
UTY transcript variant 24 NM_001258269.1:c.697= NM_001258269.1:c.697A>G
UTY transcript variant 18 NM_001258263.1:c.697= NM_001258263.1:c.697A>G
UTY transcript variant 65 NR_047635.1:n.1702= NR_047635.1:n.1702A>G
UTY transcript variant 23 NM_001258268.1:c.697= NM_001258268.1:c.697A>G
UTY transcript variant 62 NR_047632.1:n.1782= NR_047632.1:n.1782A>G
UTY transcript variant 10 NM_001258255.1:c.697= NM_001258255.1:c.697A>G
UTY transcript variant 39 NR_047609.1:n.1702= NR_047609.1:n.1702A>G
UTY transcript variant 20 NM_001258265.1:c.448= NM_001258265.1:c.448A>G
UTY transcript variant X4 XM_047442746.1:c.697= XM_047442746.1:c.697A>G
UTY transcript variant 25 NM_001258270.1:c.697= NM_001258270.1:c.697A>G
UTY transcript variant 12 NM_001258257.1:c.697= NM_001258257.1:c.697A>G
UTY transcript variant 73 NR_047643.1:n.1702= NR_047643.1:n.1702A>G
UTY transcript variant 9 NM_001258254.1:c.697= NM_001258254.1:c.697A>G
UTY transcript variant 82 NM_001400177.1:c.697= NM_001400177.1:c.697A>G
UTY transcript variant 5 NM_001258250.1:c.697= NM_001258250.1:c.697A>G
UTY transcript variant 42 NR_047612.1:n.1702= NR_047612.1:n.1702A>G
UTY transcript variant 81 NM_001400175.1:c.697= NM_001400175.1:c.697A>G
UTY transcript variant 83 NM_001400178.1:c.697= NM_001400178.1:c.697A>G
UTY transcript variant 44 NR_047614.1:n.1816= NR_047614.1:n.1816A>G
UTY transcript variant 59 NR_047629.1:n.1702= NR_047629.1:n.1702A>G
UTY transcript variant 51 NR_047621.1:n.1773= NR_047621.1:n.1773A>G
UTY transcript variant 53 NR_047623.1:n.1702= NR_047623.1:n.1702A>G
UTY transcript variant 31 NR_047601.1:n.1702= NR_047601.1:n.1702A>G
UTY transcript variant 52 NR_047622.1:n.1702= NR_047622.1:n.1702A>G
UTY transcript variant 47 NR_047617.1:n.1808= NR_047617.1:n.1808A>G
UTY transcript variant 38 NR_047608.1:n.1702= NR_047608.1:n.1702A>G
UTY transcript variant 45 NR_047615.1:n.1702= NR_047615.1:n.1702A>G
UTY transcript variant 66 NR_047636.1:n.1702= NR_047636.1:n.1702A>G
UTY transcript variant 36 NR_047606.1:n.1702= NR_047606.1:n.1702A>G
UTY transcript variant 41 NR_047611.1:n.1702= NR_047611.1:n.1702A>G
UTY transcript variant 61 NR_047631.1:n.1702= NR_047631.1:n.1702A>G
UTY transcript variant 40 NR_047610.1:n.1702= NR_047610.1:n.1702A>G
UTY transcript variant 58 NR_047628.1:n.1702= NR_047628.1:n.1702A>G
UTY transcript variant 84 NM_001400181.1:c.697= NM_001400181.1:c.697A>G
UTY transcript variant 35 NR_047605.1:n.1702= NR_047605.1:n.1702A>G
UTY transcript variant 43 NR_047613.1:n.1652= NR_047613.1:n.1652A>G
UTY transcript variant 46 NR_047616.1:n.1816= NR_047616.1:n.1816A>G
UTY transcript variant 63 NR_047633.1:n.1702= NR_047633.1:n.1702A>G
UTY transcript variant 57 NR_047627.1:n.1667= NR_047627.1:n.1667A>G
UTY transcript variant 56 NR_047626.1:n.1702= NR_047626.1:n.1702A>G
UTY transcript variant 26 NR_047596.1:n.1702= NR_047596.1:n.1702A>G
UTY transcript variant 64 NR_047634.1:n.1667= NR_047634.1:n.1667A>G
UTY transcript variant 70 NR_047640.1:n.1808= NR_047640.1:n.1808A>G
UTY transcript variant 50 NR_047620.1:n.1702= NR_047620.1:n.1702A>G
UTY transcript variant 60 NR_047630.1:n.1702= NR_047630.1:n.1702A>G
UTY transcript variant 55 NR_047625.1:n.1702= NR_047625.1:n.1702A>G
UTY transcript variant 49 NR_047619.1:n.1702= NR_047619.1:n.1702A>G
UTY transcript variant 34 NR_047604.1:n.1702= NR_047604.1:n.1702A>G
UTY transcript variant 78 NM_001400170.1:c.697= NM_001400170.1:c.697A>G
UTY transcript variant 79 NM_001400171.1:c.697= NM_001400171.1:c.697A>G
UTY transcript variant 80 NM_001400173.1:c.697= NM_001400173.1:c.697A>G
UTY transcript variant X22 XM_047442755.1:c.697= XM_047442755.1:c.697A>G
UTY transcript variant 2 NM_182659.1:c.697= NM_182659.1:c.697A>G
UTY transcript variant X23 XR_007068451.1:n.1702= XR_007068451.1:n.1702A>G
UTY transcript variant X27 XM_047442756.1:c.697= XM_047442756.1:c.697A>G
UTY transcript variant X25 XR_007068452.1:n.1702= XR_007068452.1:n.1702A>G
UTY transcript variant 92 NR_174404.1:n.1065= NR_174404.1:n.1065A>G
UTY transcript variant X28 XM_047442757.1:c.697= XM_047442757.1:c.697A>G
UTY transcript variant 93 NR_174405.1:n.1065= NR_174405.1:n.1065A>G
UTY transcript variant 1 NM_182660.1:c.697= NM_182660.1:c.697A>G
UTY transcript variant 85 NM_001400183.1:c.697= NM_001400183.1:c.697A>G
UTY transcript variant 86 NM_001400185.1:c.697= NM_001400185.1:c.697A>G
UTY transcript variant 87 NM_001400187.1:c.697= NM_001400187.1:c.697A>G
UTY transcript variant 88 NM_001400189.1:c.697= NM_001400189.1:c.697A>G
UTY transcript variant 89 NM_001400192.1:c.697= NM_001400192.1:c.697A>G
UTY transcript variant 90 NM_001400195.1:c.697= NM_001400195.1:c.697A>G
UTY transcript variant 91 NM_001400199.1:c.697= NM_001400199.1:c.697A>G
histone demethylase UTY isoform X12 XP_011529757.1:p.Asn233= XP_011529757.1:p.Asn233Asp
histone demethylase UTY isoform X10 XP_011529755.1:p.Asn233= XP_011529755.1:p.Asn233Asp
histone demethylase UTY isoform X11 XP_011529756.1:p.Asn233= XP_011529756.1:p.Asn233Asp
histone demethylase UTY isoform 3 NP_009056.3:p.Asn233= NP_009056.3:p.Asn233Asp
histone demethylase UTY isoform X1 XP_011529743.1:p.Asn233= XP_011529743.1:p.Asn233Asp
histone demethylase UTY isoform X2 XP_011529744.1:p.Asn233= XP_011529744.1:p.Asn233Asp
histone demethylase UTY isoform X3 XP_011529745.1:p.Asn233= XP_011529745.1:p.Asn233Asp
histone demethylase UTY isoform X5 XP_011529747.1:p.Asn233= XP_011529747.1:p.Asn233Asp
histone demethylase UTY isoform X6 XP_011529748.1:p.Asn233= XP_011529748.1:p.Asn233Asp
histone demethylase UTY isoform X7 XP_011529749.1:p.Asn233= XP_011529749.1:p.Asn233Asp
histone demethylase UTY isoform X8 XP_011529750.1:p.Asn233= XP_011529750.1:p.Asn233Asp
histone demethylase UTY isoform X9 XP_011529753.1:p.Asn233= XP_011529753.1:p.Asn233Asp
histone demethylase UTY isoform X21 XP_011529761.1:p.Asn233= XP_011529761.1:p.Asn233Asp
histone demethylase UTY isoform X24 XP_011529762.1:p.Asn233= XP_011529762.1:p.Asn233Asp
histone demethylase UTY isoform X23 XP_016885559.1:p.Asn233= XP_016885559.1:p.Asn233Asp
histone demethylase UTY isoform X27 XP_016885560.1:p.Asn233= XP_016885560.1:p.Asn233Asp
histone demethylase UTY isoform X28 XP_016885562.1:p.Asn233= XP_016885562.1:p.Asn233Asp
histone demethylase UTY isoform 4 NP_001245178.1:p.Asn233= NP_001245178.1:p.Asn233Asp
histone demethylase UTY isoform X14 XP_047298704.1:p.Asn233= XP_047298704.1:p.Asn233Asp
histone demethylase UTY isoform X15 XP_047298705.1:p.Asn233= XP_047298705.1:p.Asn233Asp
histone demethylase UTY isoform X17 XP_047298707.1:p.Asn233= XP_047298707.1:p.Asn233Asp
histone demethylase UTY isoform X18 XP_047298708.1:p.Asn233= XP_047298708.1:p.Asn233Asp
histone demethylase UTY isoform X20 XP_047298710.1:p.Asn233= XP_047298710.1:p.Asn233Asp
histone demethylase UTY isoform X13 XP_047298703.1:p.Asn233= XP_047298703.1:p.Asn233Asp
histone demethylase UTY isoform X16 XP_047298706.1:p.Asn233= XP_047298706.1:p.Asn233Asp
histone demethylase UTY isoform 13 NP_001245187.1:p.Asn233= NP_001245187.1:p.Asn233Asp
histone demethylase UTY isoform 7 NP_001245181.1:p.Asn233= NP_001245181.1:p.Asn233Asp
histone demethylase UTY isoform 16 NP_001245190.1:p.Asn233= NP_001245190.1:p.Asn233Asp
histone demethylase UTY isoform 15 NP_001245189.1:p.Asn233= NP_001245189.1:p.Asn233Asp
histone demethylase UTY isoform 19 NP_001245193.1:p.Asn233= NP_001245193.1:p.Asn233Asp
histone demethylase UTY isoform 21 NP_001245195.1:p.Asn233= NP_001245195.1:p.Asn233Asp
histone demethylase UTY isoform X19 XP_047298709.1:p.Asn233= XP_047298709.1:p.Asn233Asp
histone demethylase UTY isoform 6 NP_001245180.1:p.Asn233= NP_001245180.1:p.Asn233Asp
histone demethylase UTY isoform 22 NP_001245196.1:p.Asn233= NP_001245196.1:p.Asn233Asp
histone demethylase UTY isoform 11 NP_001245185.1:p.Asn233= NP_001245185.1:p.Asn233Asp
histone demethylase UTY isoform 14 NP_001245188.1:p.Asn233= NP_001245188.1:p.Asn233Asp
histone demethylase UTY isoform 17 NP_001245191.1:p.Asn233= NP_001245191.1:p.Asn233Asp
histone demethylase UTY isoform 8 NP_001245182.1:p.Asn233= NP_001245182.1:p.Asn233Asp
histone demethylase UTY isoform 24 NP_001245198.1:p.Asn233= NP_001245198.1:p.Asn233Asp
histone demethylase UTY isoform 18 NP_001245192.1:p.Asn233= NP_001245192.1:p.Asn233Asp
histone demethylase UTY isoform 23 NP_001245197.1:p.Asn233= NP_001245197.1:p.Asn233Asp
histone demethylase UTY isoform 10 NP_001245184.1:p.Asn233= NP_001245184.1:p.Asn233Asp
histone demethylase UTY isoform 20 NP_001245194.1:p.Asn150= NP_001245194.1:p.Asn150Asp
histone demethylase UTY isoform X4 XP_047298702.1:p.Asn233= XP_047298702.1:p.Asn233Asp
histone demethylase UTY isoform 25 NP_001245199.1:p.Asn233= NP_001245199.1:p.Asn233Asp
histone demethylase UTY isoform 12 NP_001245186.1:p.Asn233= NP_001245186.1:p.Asn233Asp
histone demethylase UTY isoform 9 NP_001245183.1:p.Asn233= NP_001245183.1:p.Asn233Asp
histone demethylase UTY isoform 30 NP_001387106.1:p.Asn233= NP_001387106.1:p.Asn233Asp
histone demethylase UTY isoform 5 NP_001245179.1:p.Asn233= NP_001245179.1:p.Asn233Asp
histone demethylase UTY isoform 29 NP_001387104.1:p.Asn233= NP_001387104.1:p.Asn233Asp
histone demethylase UTY isoform 31 NP_001387107.1:p.Asn233= NP_001387107.1:p.Asn233Asp
histone demethylase UTY isoform 32 NP_001387110.1:p.Asn233= NP_001387110.1:p.Asn233Asp
histone demethylase UTY isoform 26 NP_001387099.1:p.Asn233= NP_001387099.1:p.Asn233Asp
histone demethylase UTY isoform 27 NP_001387100.1:p.Asn233= NP_001387100.1:p.Asn233Asp
histone demethylase UTY isoform 28 NP_001387102.1:p.Asn233= NP_001387102.1:p.Asn233Asp
histone demethylase UTY isoform X22 XP_047298711.1:p.Asn233= XP_047298711.1:p.Asn233Asp
histone demethylase UTY isoform 2 NP_872600.1:p.Asn233= NP_872600.1:p.Asn233Asp
histone demethylase UTY isoform X25 XP_047298712.1:p.Asn233= XP_047298712.1:p.Asn233Asp
histone demethylase UTY isoform X26 XP_047298713.1:p.Asn233= XP_047298713.1:p.Asn233Asp
histone demethylase UTY isoform 1 NP_872601.1:p.Asn233= NP_872601.1:p.Asn233Asp
histone demethylase UTY isoform 33 NP_001387112.1:p.Asn233= NP_001387112.1:p.Asn233Asp
histone demethylase UTY isoform 34 NP_001387114.1:p.Asn233= NP_001387114.1:p.Asn233Asp
histone demethylase UTY isoform 35 NP_001387116.1:p.Asn233= NP_001387116.1:p.Asn233Asp
histone demethylase UTY isoform 36 NP_001387118.1:p.Asn233= NP_001387118.1:p.Asn233Asp
histone demethylase UTY isoform 37 NP_001387121.1:p.Asn233= NP_001387121.1:p.Asn233Asp
histone demethylase UTY isoform 38 NP_001387124.1:p.Asn233= NP_001387124.1:p.Asn233Asp
histone demethylase UTY isoform 39 NP_001387128.1:p.Asn233= NP_001387128.1:p.Asn233Asp
UTY transcript variant X39 XM_005262556.1:c.217-32963= XM_005262556.1:c.217-32963A>G
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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 ss2745636848 Nov 08, 2017 (151)
2 gnomAD - Exomes NC_000024.9 - 15481178 Jul 14, 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
14965460, ss2745636848 NC_000024.9:15481177:T:C NC_000024.10:13369297: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 rs1474835561

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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