Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: MCMDC2 (Hsa)
(GRCh38)8:66874171C>T
(Homo sapiens)Allele/Variant
Source: rs1811159019
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66874171C>T
(GRCh38)8:66905227G>A
(Homo sapiens)Allele/Variant
Source: rs201352762
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66905227G>A
(GRCh38)8:66877433T>G
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.66877433T>G
Genes: MCMDC2 (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)8:66877433T>G
(GRCh38)8:66896795C>G
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.66896795C>G
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66896795C>G
(GRCh38)8:66919058T>G
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.66919058T>G
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66919058T>G
(GRCh38)8:66905251C>T
(Homo sapiens)Allele/Variant
Source: rs370115455
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66905251C>T
(GRCh38)8:66878673A>G
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.66878673A>G
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66878673A>G
(GRCh38)8:66901311T>G
(Homo sapiens)Allele/Variant
Source: rs145255251
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66901311T>G
(GRCh38)8:66874571G>T
(Homo sapiens)Allele/Variant
Source: rs781559154
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66874571G>T
(GRCh38)8:66883796C>G
(Homo sapiens)Allele/Variant
Source: rs377744254
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883796C>G
(GRCh38)8:66883928G>A
(Homo sapiens)Allele/Variant
Source: rs140963222
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883928G>A
(GRCh38)8:66878865G>A
(Homo sapiens)Allele/Variant
Source: rs753555437
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66878865G>A
(GRCh38)8:66874223A>G
(Homo sapiens)Allele/Variant
Source: rs1811161564
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66874223A>G
(GRCh38)8:66896939A>G
(Homo sapiens)Allele/Variant
Source: rs768605665
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66896939A>G
(GRCh38)8:66883909C>G
(Homo sapiens)Allele/Variant
Source: rs144829606
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883909C>G
(GRCh38)8:66896903C>T
(Homo sapiens)Allele/Variant
Source: rs35871529
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66896903C>T
(GRCh38)8:66877397G>A
(Homo sapiens)Allele/Variant
Source: rs367891525
Genes: MCMDC2 (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)8:66877397G>A
(GRCh38)8:66883834C>T
(Homo sapiens)Allele/Variant
Source: rs773320366
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883834C>T
(GRCh38)8:66890897G>A
(Homo sapiens)Allele/Variant
Source: rs779816268
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66890897G>A
(GRCh38)8:66896942A>G
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.66896942A>G
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66896942A>G
(GRCh38)8:66919119T>G
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.66919119T>G
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66919119T>G
(GRCh38)8:66890892C>A
(Homo sapiens)Allele/Variant
Source: rs112645348
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66890892C>A
(GRCh38)8:66877506G>C
(Homo sapiens)Allele/Variant
Source: rs145983403
Genes: MCMDC2 (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)8:66877506G>C
(GRCh38)8:66883856A>T
(Homo sapiens)Allele/Variant
Source: rs369758604
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883856A>T
(GRCh38)8:66890974A>G
(Homo sapiens)Allele/Variant
Source: rs561670232
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66890974A>G
(GRCh38)8:66880905A>T
(Homo sapiens)Allele/Variant
Source: rs760279097
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66880905A>T
(GRCh38)8:66896897A>G
(Homo sapiens)Allele/Variant
Source: rs562391447
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66896897A>G
(GRCh38)8:66878585A>T
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.66878585A>T
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66878585A>T
(GRCh38)8:66878928A>G
(Homo sapiens)Allele/Variant
Source: rs181029958
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66878928A>G
(GRCh38)8:66883865C>G
(Homo sapiens)Allele/Variant
Source: rs765329862
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883865C>G
(GRCh38)8:66896177G>T
(Homo sapiens)Allele/Variant
Source: rs368649010
Genes: MCMDC2 (Hsa), SNHG6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66896177G>T
(GRCh38)8:66890906G>A
(Homo sapiens)Allele/Variant
Source: rs373658749
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66890906G>A
(GRCh38)8:66896253C>T
(Homo sapiens)Allele/Variant
Source: rs751075073
Genes: MCMDC2 (Hsa), SNHG6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66896253C>T
(GRCh38)8:66896811A>G
(Homo sapiens)Allele/Variant
Source: rs1812374448
Genes: MCMDC2 (Hsa), SNHG6 (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)8:66896811A>G
(GRCh38)8:66901346T>A
(Homo sapiens)Allele/Variant
Source: rs143895635
Genes: MCMDC2 (Hsa), SNHG6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66901346T>A