Version: 8.0.0
Date: Tue Jan 28 2025
7 results for groa
Allele/Variant

(GRCh38)4:73869752G>A

(Homo sapiens)
Allele/Variant
Source: rs186092967
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869752G>A
Gene Synonyms: GROa

(GRCh38)4:73869777C>T

(Homo sapiens)
Allele/Variant
Source: rs145342393
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869777C>T
Gene Synonyms: GROa

(GRCh38)4:73869498C>T

(Homo sapiens)
Allele/Variant
Source: NC_000004.12:g.73869498C>T
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869498C>T
Gene Synonyms: GROa

(GRCh38)4:73869698C>G

(Homo sapiens)
Allele/Variant
Source: NC_000004.12:g.73869698C>G
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869698C>G
Gene Synonyms: GROa

(GRCh38)4:73869716C>A

(Homo sapiens)
Allele/Variant
Source: rs200234866
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869716C>A
Gene Synonyms: GROa

(GRCh38)4:73869738T>C

(Homo sapiens)
Allele/Variant
Source: rs201545979
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869738T>C
Gene Synonyms: GROa

(GRCh38)4:73869751C>G

(Homo sapiens)
Allele/Variant
Source: rs201293315
Genes: CXCL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:73869751C>G
Gene Synonyms: GROa