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

(GRCh38)6:29942944G>A

(Homo sapiens)
Allele/Variant
Source: rs199474424
Genes: HLA-A (Hsa), POLR1HASP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:29942944G>A

(GRCh38)6:29943261G>A

(Homo sapiens)
Allele/Variant
Source: rs41554914
Genes: HLA-A (Hsa), POLR1HASP (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)6:29943261G>A

(GRCh38)6:29941373A>G

(Homo sapiens)
Allele/Variant
Source: rs1370973378
Genes: HLA-A (Hsa), POLR1HASP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:29941373A>G

(GRCh38)6:29944160G>C

(Homo sapiens)
Allele/Variant
Source: rs281864764
Genes: HLA-A (Hsa), POLR1HASP (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)6:29944160G>C

(GRCh38)6:29942772G>A

(Homo sapiens)
Allele/Variant
Source: rs45585732
Genes: HLA-A (Hsa), POLR1HASP (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)6:29942772G>A

(GRCh38)6:29948263G>A

(Homo sapiens)
Allele/Variant
Source: rs9256984
Genes: HLA-A (Hsa), POLR1HASP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:29948263G>A

(GRCh38)6:29943307G>A

(Homo sapiens)
Allele/Variant
Source: rs199474493
Genes: HLA-A (Hsa), POLR1HASP (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)6:29943307G>A

(GRCh38)6:29945521A>T

(Homo sapiens)
Allele/Variant
Source: rs1061235
Genes: HLA-A (Hsa), POLR1HASP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)6:29945521A>T

(GRCh38)6:29945230C>T

(Homo sapiens)
Allele/Variant
Source: rs200140272
Genes: HLA-A (Hsa), POLR1HASP (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)6:29945230C>T