Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: RPL36A-HNRNPH2 (Hsa)
(GRCh38)X:101397938G>C
(Homo sapiens)Allele/Variant
Source: rs2147470731
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101397938G>C
(GRCh38)X:101397943G>A
(Homo sapiens)Allele/Variant
Source: rs869312233
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101397943G>A
(GRCh38)X:101397945G>T
(Homo sapiens)Allele/Variant
Source: rs1555984780
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101397945G>T
(GRCh38)X:101398411T>G
(Homo sapiens)Allele/Variant
Source: rs1555984950
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398411T>G
(GRCh38)X:101398451T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101398451T>C
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398451T>C
(GRCh38)X:101398056G>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101398056G>T
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398056G>T
(GRCh38)X:101398077T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101398077T>G
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398077T>G
(GRCh38)X:101400667T>G
(Homo sapiens)Allele/Variant
Source: rs869312149
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101400667T>G
(GRCh38)X:101398481C>A
(Homo sapiens)Allele/Variant
Source: rs104894846
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398481C>A
(GRCh38)X:101403819C>G
(Homo sapiens)Allele/Variant
Source: rs782197638
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101403819C>G
(GRCh38)X:101407910G>A
(Homo sapiens)Allele/Variant
Source: rs782637185
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407910G>A
(GRCh38)X:101407911G>C
(Homo sapiens)Allele/Variant
Source: rs371291716
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407911G>C
(GRCh38)X:101407912T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101407912T>G
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407912T>G
(GRCh38)X:101407935C>T
(Homo sapiens)Allele/Variant
Source: rs1057523740
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407935C>T
(GRCh38)X:101398496A>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101398496A>G
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398496A>G
(GRCh38)X:101403800T>C
(Homo sapiens)Allele/Variant
Source: rs1555986227
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101403800T>C
(GRCh38)X:101398504T>A
(Homo sapiens)Allele/Variant
Source: rs140329381
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398504T>A
(GRCh38)X:101398784C>G
(Homo sapiens)Allele/Variant
Source: rs868923658
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398784C>G
(GRCh38)X:101398785C>T
(Homo sapiens)Allele/Variant
Source: rs730880451
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398785C>T
(GRCh38)X:101398558C>T
(Homo sapiens)Allele/Variant
Source: rs1928174707
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398558C>T
(GRCh38)X:101407916C>G
(Homo sapiens)Allele/Variant
Source: rs782051708
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407916C>G
(GRCh38)X:101407947G>C
(Homo sapiens)Allele/Variant
Source: rs781906252
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407947G>C
(GRCh38)X:101398054A>G
(Homo sapiens)Allele/Variant
Source: rs1928137126
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398054A>G
(GRCh38)X:101398363T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101398363T>G
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398363T>G
(GRCh38)X:101397934G>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101397934G>C
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101397934G>C
(GRCh38)X:101398925G>A
(Homo sapiens)Allele/Variant
Source: rs797044747
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398925G>A
(GRCh38)X:101398962T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101398962T>G
Genes: RPL36A-HNRNPH2 (Hsa), GLA (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)X:101398962T>G
(GRCh38)X:101398498C>T
(Homo sapiens)Allele/Variant
Source: rs869312439
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398498C>T
(GRCh38)X:101398499C>T
(Homo sapiens)Allele/Variant
Source: rs869312438
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398499C>T
(GRCh38)X:101398508C>A
(Homo sapiens)Allele/Variant
Source: rs104894839
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398508C>A
(GRCh38)X:101407927A>C
(Homo sapiens)Allele/Variant
Source: rs1603048396
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407927A>C
(GRCh38)X:101407913G>A
(Homo sapiens)Allele/Variant
Source: rs2071225
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407913G>A
(GRCh38)X:101407933C>T
(Homo sapiens)Allele/Variant
Source: rs3027584
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407933C>T
(GRCh38)X:101397990G>A
(Homo sapiens)Allele/Variant
Source: rs2147470905
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101397990G>A
(GRCh38)X:101398449G>A
(Homo sapiens)Allele/Variant
Source: rs869312447
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398449G>A
(GRCh38)X:101398074C>T
(Homo sapiens)Allele/Variant
Source: rs28935493
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398074C>T
(GRCh38)X:101397860A>G
(Homo sapiens)Allele/Variant
Source: rs782058162
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101397860A>G
(GRCh38)X:101397906T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101397906T>G
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101397906T>G
(GRCh38)X:101398787T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101398787T>C
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398787T>C
(GRCh38)X:101398538C>G
(Homo sapiens)Allele/Variant
Source: rs782196174
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398538C>G
(GRCh38)X:101398454A>G
(Homo sapiens)Allele/Variant
Source: rs782250167
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398454A>G
(GRCh38)X:101400732C>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101400732C>G
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101400732C>G
(GRCh38)X:101398470A>G
(Homo sapiens)Allele/Variant
Source: rs398123223
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398470A>G
(GRCh38)X:101401777A>C
(Homo sapiens)Allele/Variant
Source: rs1183869568
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101401777A>C
(GRCh38)X:101403909T>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101403909T>G
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101403909T>G
(GRCh38)X:101401699A>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.101401699A>T
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101401699A>T
(GRCh38)X:101401757G>A
(Homo sapiens)Allele/Variant
Source: rs886044843
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101401757G>A
(GRCh38)X:101398795T>A
(Homo sapiens)Allele/Variant
Source: rs28935486
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398795T>A
(GRCh38)X:101398891A>C
(Homo sapiens)Allele/Variant
Source: rs797044749
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101398891A>C
(GRCh38)X:101407751C>T
(Homo sapiens)Allele/Variant
Source: rs869312255
Genes: RPL36A-HNRNPH2 (Hsa), GLA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:101407751C>T