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

(GRCh38)10:86960103C>T

(Homo sapiens)
Allele/Variant
Source: rs770502987
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86960103C>T

(GRCh38)10:86960033G>C

(Homo sapiens)
Allele/Variant
Source: NC_000010.11:g.86960033G>C
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86960033G>C

(GRCh38)10:86962974G>A

(Homo sapiens)
Allele/Variant
Source: rs374301169
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86962974G>A

(GRCh38)10:86962637G>A

(Homo sapiens)
Allele/Variant
Source: rs267602604
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86962637G>A

(GRCh38)10:86958727C>A

(Homo sapiens)
Allele/Variant
Source: rs74150417
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86958727C>A

(GRCh38)10:86962974G>T

(Homo sapiens)
Allele/Variant
Source: rs374301169
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86962974G>T

(GRCh38)10:86960124G>A

(Homo sapiens)
Allele/Variant
Source: rs371074090
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86960124G>A

(GRCh38)10:86962661G>C

(Homo sapiens)
Allele/Variant
Source: rs779800178
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86962661G>C

(GRCh38)10:86960116G>A

(Homo sapiens)
Allele/Variant
Source: rs111800178
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86960116G>A

(GRCh38)10:86960057G>A

(Homo sapiens)
Allele/Variant
Source: rs144819543
Genes: MMRN2 (Hsa), SNCG (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:86960057G>A