Version: 8.0.0
Date: Tue Jan 28 2025
19 results
Allele/Variant Genes: MCMDC2 (Hsa) Molecular Consequence: non coding transcript variant

(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)8:66878673A>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)8:66874571G>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)8:66883909C>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)8:66883834C>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)8:66890892C>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)8:66883856A>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)8:66878585A>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)8:66883865C>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