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

(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)8:66901311T>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)8:66896939A>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)8:66896903C>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)8:66901346T>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

(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)8:66877506G>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)8:66896897A>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)8:66878928A>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)8:66896811A>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