15 results for apr3
Allele/Variant Molecular Consequence: intron variant

(GRCh38)2:27215521G>A

(Homo sapiens)
Allele/Variant
Source: rs774832372
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215521G>A
Gene Synonyms: APR3

(GRCh38)2:27215699G>T

(Homo sapiens)
Allele/Variant
Source: rs571082250
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215699G>T
Gene Synonyms: APR3

(GRCh38)2:27215648G>C

(Homo sapiens)
Allele/Variant
Source: rs776772424
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215648G>C
Gene Synonyms: APR3

(GRCh38)2:27216937A>G

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.27216937A>G
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216937A>G
Gene Synonyms: APR3

(GRCh38)2:27216598A>T

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.27216598A>T
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216598A>T
Gene Synonyms: APR3

(GRCh38)2:27213202T>C

(Homo sapiens)
Allele/Variant
Source: rs201877637
Genes: ATRAID (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)2:27213202T>C
Gene Synonyms: APR3

(GRCh38)2:27213222G>C

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.27213222G>C
Genes: ATRAID (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)2:27213222G>C
Gene Synonyms: APR3

(GRCh38)2:27216546T>C

(Homo sapiens)
Allele/Variant
Source: rs201778106
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216546T>C
Gene Synonyms: APR3

(GRCh38)2:27215724A>G

(Homo sapiens)
Allele/Variant
Source: rs779575892
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215724A>G
Gene Synonyms: APR3

(GRCh38)2:27215520C>T

(Homo sapiens)
Allele/Variant
Source: rs147821107
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215520C>T
Gene Synonyms: APR3

(GRCh38)2:27215735A>G

(Homo sapiens)
Allele/Variant
Source: rs369720973
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215735A>G
Gene Synonyms: APR3

(GRCh38)2:27215742C>G

(Homo sapiens)
Allele/Variant
Source: rs748140857
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215742C>G
Gene Synonyms: APR3

(GRCh38)2:27216929G>A

(Homo sapiens)
Allele/Variant
Source: rs148460328
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216929G>A
Gene Synonyms: APR3

(GRCh38)2:27216904A>T

(Homo sapiens)
Allele/Variant
Source: rs1674869385
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27216904A>T
Gene Synonyms: APR3

(GRCh38)2:27215499G>A

(Homo sapiens)
Allele/Variant
Source: rs147492156
Genes: ATRAID (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:27215499G>A
Gene Synonyms: APR3