Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: INHA (Hsa)
(GRCh38)2:219572569G>T
(Homo sapiens)Allele/Variant
Source: rs34400751
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219572569G>T
(GRCh38)2:219575369C>T
(Homo sapiens)Allele/Variant
Source: rs1697502198
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219575369C>T
(GRCh38)2:219574752C>T
(Homo sapiens)Allele/Variant
Source: rs36032184
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219574752C>T
(GRCh38)2:219574789C>T
(Homo sapiens)Allele/Variant
Source: rs577636996
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219574789C>T
(GRCh38)2:219572581C>T
(Homo sapiens)Allele/Variant
Source: rs371366906
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219572581C>T
(GRCh38)2:219574904G>C
(Homo sapiens)Allele/Variant
Source: rs746904695
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219574904G>C
(GRCh38)2:219575194G>A
(Homo sapiens)Allele/Variant
Source: rs12720062
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219575194G>A
(GRCh38)2:219572451G>A
(Homo sapiens)Allele/Variant
Source: rs746580263
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219572451G>A
(GRCh38)2:219572503C>T
(Homo sapiens)Allele/Variant
Source: rs141940534
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219572503C>T
(GRCh38)2:219574936C>T
(Homo sapiens)Allele/Variant
Source: rs759167075
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219574936C>T
(GRCh38)2:219574808C>T
(Homo sapiens)Allele/Variant
Source: rs748024269
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219574808C>T
(GRCh38)2:219574867T>G
(Homo sapiens)Allele/Variant
Source: rs374088703
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219574867T>G
(GRCh38)2:219575183C>T
(Homo sapiens)Allele/Variant
Source: rs750272026
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219575183C>T
(GRCh38)2:219572359C>T
(Homo sapiens)Allele/Variant
Source: rs35118453
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219572359C>T
(GRCh38)2:219572541G>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219572541G>T
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219572541G>T
(GRCh38)2:219574856C>T
(Homo sapiens)Allele/Variant
Source: rs1559166359
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219574856C>T
(GRCh38)2:219575172G>A
(Homo sapiens)Allele/Variant
Source: rs140014760
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219575172G>A
(GRCh38)2:219572507G>A
(Homo sapiens)Allele/Variant
Source: rs753969684
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219572507G>A
(GRCh38)2:219570580G>A
(Homo sapiens)Allele/Variant
Source: rs1182793569
Genes: INHA (Hsa), OBSL1 (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)2:219570580G>A
(GRCh38)2:219570931A>T
(Homo sapiens)Allele/Variant
Source: rs2106118426
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219570931A>T
(GRCh38)2:219570255G>C
(Homo sapiens)Allele/Variant
Source: rs2106112941
Genes: INHA (Hsa), OBSL1 (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)2:219570255G>C
(GRCh38)2:219570518C>T
(Homo sapiens)Allele/Variant
Source: rs2106115186
Genes: INHA (Hsa), OBSL1 (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)2:219570518C>T
(GRCh38)2:219570271G>A
(Homo sapiens)Allele/Variant
Source: rs750505464
Genes: INHA (Hsa), OBSL1 (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)2:219570271G>A
(GRCh38)2:219570866A>G
(Homo sapiens)Allele/Variant
Source: rs748291209
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219570866A>G
(GRCh38)2:219570357G>A
(Homo sapiens)Allele/Variant
Source: rs551084552
Genes: INHA (Hsa), OBSL1 (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)2:219570357G>A
(GRCh38)2:219570468G>A
(Homo sapiens)Allele/Variant
Source: rs751927713
Genes: INHA (Hsa), OBSL1 (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)2:219570468G>A
(GRCh38)2:219571045T>C
(Homo sapiens)Allele/Variant
Source: rs1364672065
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219571045T>C
(GRCh38)2:219571110A>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219571110A>T
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219571110A>T
(GRCh38)2:219570255G>A
(Homo sapiens)Allele/Variant
Source: rs2106112941
Genes: INHA (Hsa), OBSL1 (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)2:219570255G>A
(GRCh38)2:219570640G>T
(Homo sapiens)Allele/Variant
Source: rs186348476
Genes: INHA (Hsa), OBSL1 (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)2:219570640G>T
(GRCh38)2:219575153C>G
(Homo sapiens)Allele/Variant
Source: rs376758084
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219575153C>G
(GRCh38)2:219570542C>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219570542C>A
Genes: INHA (Hsa), OBSL1 (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)2:219570542C>A
(GRCh38)2:219570634C>G
(Homo sapiens)Allele/Variant
Source: rs2106116161
Genes: INHA (Hsa), OBSL1 (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)2:219570634C>G
(GRCh38)2:219570664G>C
(Homo sapiens)Allele/Variant
Source: rs148433261
Genes: INHA (Hsa), OBSL1 (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)2:219570664G>C
(GRCh38)2:219570676T>C
(Homo sapiens)Allele/Variant
Source: rs886055667
Genes: INHA (Hsa), OBSL1 (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)2:219570676T>C
(GRCh38)2:219570789C>T
(Homo sapiens)Allele/Variant
Source: rs2106117284
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219570789C>T
(GRCh38)2:219571158A>C
(Homo sapiens)Allele/Variant
Source: rs376818200
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219571158A>C
(GRCh38)2:219571283T>A
(Homo sapiens)Allele/Variant
Source: rs796511004
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219571283T>A
(GRCh38)2:219574957G>A
(Homo sapiens)Allele/Variant
Source: rs372427524
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219574957G>A
(GRCh38)2:219575021G>A
(Homo sapiens)Allele/Variant
Source: rs367749891
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219575021G>A
(GRCh38)2:219575131C>G
(Homo sapiens)Allele/Variant
Source: rs200600232
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219575131C>G
(GRCh38)2:219575429T>C
(Homo sapiens)Allele/Variant
Source: rs140659175
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219575429T>C
(GRCh38)2:219575447G>A
(Homo sapiens)Allele/Variant
Source: rs777288649
Genes: INHA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219575447G>A
(GRCh38)2:219571244A>G
(Homo sapiens)Allele/Variant
Source: rs781320979
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219571244A>G
(GRCh38)2:219571441G>C
(Homo sapiens)Allele/Variant
Source: rs529852516
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219571441G>C
(GRCh38)2:219570807C>G
(Homo sapiens)Allele/Variant
Source: rs764783588
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219570807C>G
(GRCh38)2:219570992C>A
(Homo sapiens)Allele/Variant
Source: rs775129122
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219570992C>A
(GRCh38)2:219571024A>G
(Homo sapiens)Allele/Variant
Source: rs1404629311
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219571024A>G
(GRCh38)2:219571097C>G
(Homo sapiens)Allele/Variant
Source: rs1026599495
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219571097C>G
(GRCh38)2:219571172C>T
(Homo sapiens)Allele/Variant
Source: rs563828175
Genes: INHA (Hsa), OBSL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219571172C>T