Version: 8.1.0
Date: Fri Apr 18 2025
19 results for R3HDML-AS1

R3HDML-AS1

(Homo sapiens)
Gene
Name: R3HDML antisense RNA 1
Synonyms: uncharacterized LOC105372629, LOC105372629
Source: HGNC:55830
Biotype: ncRNA gene
Symbol: R3HDML-AS1 (Hsa)
Symbol: R3HDML-AS1

(GRCh38)20:44355404G>A

(Homo sapiens)
Allele/Variant
Source: rs537336047
Genes: R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44355404G>A

(GRCh38)20:44355379C>G

(Homo sapiens)
Allele/Variant
Source: rs1193282686
Genes: R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44355379C>G

(GRCh38)20:44355427T>A

(Homo sapiens)
Allele/Variant
Source: rs1048936817
Genes: R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44355427T>A

(GRCh38)20:44355240T>C

(Homo sapiens)
Allele/Variant
Source: rs377144780
Genes: R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44355240T>C

(GRCh38)20:44355527G>A

(Homo sapiens)
Allele/Variant
Source: rs112444447
Genes: R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44355527G>A

(GRCh38)20:44355221A>T

(Homo sapiens)
Allele/Variant
Source: rs149135843
Genes: R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44355221A>T

(GRCh38)20:44355529G>T

(Homo sapiens)
Allele/Variant
Source: rs148318607
Genes: R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44355529G>T

(GRCh38)20:44350676G>A

(Homo sapiens)
Allele/Variant
Source: rs746791288
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44350676G>A

(GRCh38)20:44343499A>G

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.44343499A>G
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44343499A>G

(GRCh38)20:44345324T>G

(Homo sapiens)
Allele/Variant
Source: rs544966671
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44345324T>G

(GRCh38)20:44345266G>A

(Homo sapiens)
Allele/Variant
Source: rs377253823
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44345266G>A

(GRCh38)20:44345371G>A

(Homo sapiens)
Allele/Variant
Source: rs2062783658
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44345371G>A

(GRCh38)20:44341311G>A

(Homo sapiens)
Allele/Variant
Source: rs1266833548
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44341311G>A

(GRCh38)20:44341221C>A

(Homo sapiens)
Allele/Variant
Source: rs749580720
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44341221C>A

(GRCh38)20:44341199T>A

(Homo sapiens)
Allele/Variant
Source: NC_000020.11:g.44341199T>A
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44341199T>A

(GRCh38)20:44343474C>T

(Homo sapiens)
Allele/Variant
Source: rs375142726
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44343474C>T

(GRCh38)20:44343480G>A

(Homo sapiens)
Allele/Variant
Source: rs112634290
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44343480G>A

(GRCh38)20:44350683C>T

(Homo sapiens)
Allele/Variant
Source: rs369678042
Genes: R3HDML (Hsa), R3HDML-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)20:44350683C>T