Version: 8.0.0
Date: Tue Jan 28 2025
9 results
Allele/Variant Genes: EMC3 (Hsa)

(GRCh38)3:9964111G>A

(Homo sapiens)
Allele/Variant
Source: rs769523238
Genes: EMC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:9964111G>A

(GRCh38)3:9986533C>G

(Homo sapiens)
Allele/Variant
Source: rs373587570
Genes: EMC3 (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)3:9986533C>G

(GRCh38)3:9986541C>G

(Homo sapiens)
Allele/Variant
Source: rs2085974749
Genes: EMC3 (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)3:9986541C>G

(GRCh38)3:10007364G>C

(Homo sapiens)
Allele/Variant
Source: rs565282870
Genes: EMC3 (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)3:10007364G>C

(GRCh38)3:9977432C>T

(Homo sapiens)
Allele/Variant
Source: NC_000003.12:g.9977432C>T
Genes: EMC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:9977432C>T

(GRCh38)3:9969742C>T

(Homo sapiens)
Allele/Variant
Source: rs761023207
Genes: EMC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:9969742C>T

(GRCh38)3:9986547G>C

(Homo sapiens)
Allele/Variant
Source: rs1319989898
Genes: EMC3 (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)3:9986547G>C

(GRCh38)3:10007622C>T

(Homo sapiens)
Allele/Variant
Source: rs1263502200
Genes: EMC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:10007622C>T

(GRCh38)3:9970618G>A

(Homo sapiens)
Allele/Variant
Source: rs2085775340
Genes: EMC3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:9970618G>A