Version: 8.1.0
Date: Fri Apr 18 2025
101 results for PRKAG2-AS1

PRKAG2-AS1

(Homo sapiens)
Gene
Name: PRKAG2 antisense RNA 1
Synonyms: RP11-796I2.2
Source: HGNC:40468
Biotype: ncRNA gene
Symbol: PRKAG2-AS1 (Hsa)
Symbol: PRKAG2-AS1

(GRCh38)7:151877389C>G

(Homo sapiens)
Allele/Variant
Source: rs147892513
Genes: PRKAG2-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151877389C>G

(GRCh38)7:151877573C>T

(Homo sapiens)
Allele/Variant
Source: rs28413951
Genes: PRKAG2-AS1 (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)7:151877573C>T

(GRCh38)7:151877195G>A

(Homo sapiens)
Allele/Variant
Source: rs886062108
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151877195G>A

(GRCh38)7:151876538T>C

(Homo sapiens)
Allele/Variant
Source: rs1164114205
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876538T>C

(GRCh38)7:151876565C>T

(Homo sapiens)
Allele/Variant
Source: rs368522976
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876565C>T

(GRCh38)7:151876595T>A

(Homo sapiens)
Allele/Variant
Source: rs574029693
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876595T>A

(GRCh38)7:151876598G>A

(Homo sapiens)
Allele/Variant
Source: NC_000007.14:g.151876598G>A
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876598G>A

(GRCh38)7:151876699G>C

(Homo sapiens)
Allele/Variant
Source: rs565170478
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876699G>C

(GRCh38)7:151876971C>T

(Homo sapiens)
Allele/Variant
Source: rs886062105
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876971C>T

(GRCh38)7:151876555G>T

(Homo sapiens)
Allele/Variant
Source: NC_000007.14:g.151876555G>T
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876555G>T

(GRCh38)7:151876577G>A

(Homo sapiens)
Allele/Variant
Source: rs1306017686
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876577G>A

(GRCh38)7:151876514T>C

(Homo sapiens)
Allele/Variant
Source: rs2080409943
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876514T>C

(GRCh38)7:151876508G>A

(Homo sapiens)
Allele/Variant
Source: rs984007665
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876508G>A

(GRCh38)7:151876534C>T

(Homo sapiens)
Allele/Variant
Source: rs2080410736
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876534C>T

(GRCh38)7:151876555G>A

(Homo sapiens)
Allele/Variant
Source: rs730880971
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876555G>A

(GRCh38)7:151876617C>T

(Homo sapiens)
Allele/Variant
Source: NC_000007.14:g.151876617C>T
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876617C>T

(GRCh38)7:151876557C>T

(Homo sapiens)
Allele/Variant
Source: rs1057524523
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876557C>T

(GRCh38)7:151876561G>A

(Homo sapiens)
Allele/Variant
Source: rs745416806
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876561G>A

(GRCh38)7:151876621A>G

(Homo sapiens)
Allele/Variant
Source: rs370949737
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876621A>G

(GRCh38)7:151876632G>C

(Homo sapiens)
Allele/Variant
Source: rs765372069
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876632G>C

(GRCh38)7:151876659G>T

(Homo sapiens)
Allele/Variant
Source: rs1554622689
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876659G>T

(GRCh38)7:151876597G>T

(Homo sapiens)
Allele/Variant
Source: rs1316860428
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876597G>T

(GRCh38)7:151876555G>C

(Homo sapiens)
Allele/Variant
Source: rs730880971
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876555G>C

(GRCh38)7:151876650C>T

(Homo sapiens)
Allele/Variant
Source: rs751906842
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876650C>T

(GRCh38)7:151877180G>A

(Homo sapiens)
Allele/Variant
Source: rs117728810
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151877180G>A

(GRCh38)7:151876590T>C

(Homo sapiens)
Allele/Variant
Source: rs1041124171
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876590T>C

(GRCh38)7:151876578A>G

(Homo sapiens)
Allele/Variant
Source: rs1563775284
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876578A>G

(GRCh38)7:151876612G>A

(Homo sapiens)
Allele/Variant
Source: rs771101951
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876612G>A

(GRCh38)7:151876636T>C

(Homo sapiens)
Allele/Variant
Source: rs200468798
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876636T>C

(GRCh38)7:151876589T>A

(Homo sapiens)
Allele/Variant
Source: rs1060503025
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876589T>A

(GRCh38)7:151876530G>C

(Homo sapiens)
Allele/Variant
Source: rs751957422
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876530G>C

(GRCh38)7:151876511A>G

(Homo sapiens)
Allele/Variant
Source: NC_000007.14:g.151876511A>G
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876511A>G

(GRCh38)7:151876513G>C

(Homo sapiens)
Allele/Variant
Source: rs753210415
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876513G>C

(GRCh38)7:151876575T>A

(Homo sapiens)
Allele/Variant
Source: rs1444086983
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876575T>A

(GRCh38)7:151876537C>T

(Homo sapiens)
Allele/Variant
Source: rs1586767586
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876537C>T

(GRCh38)7:151876570G>A

(Homo sapiens)
Allele/Variant
Source: NC_000007.14:g.151876570G>A
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876570G>A

(GRCh38)7:151876579A>T

(Homo sapiens)
Allele/Variant
Source: rs141316327
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876579A>T

(GRCh38)7:151876594C>T

(Homo sapiens)
Allele/Variant
Source: rs1243792222
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876594C>T

(GRCh38)7:151876507C>T

(Homo sapiens)
Allele/Variant
Source: rs397517261
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876507C>T

(GRCh38)7:151876569C>A

(Homo sapiens)
Allele/Variant
Source: rs1282017092
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876569C>A

(GRCh38)7:151876515G>A

(Homo sapiens)
Allele/Variant
Source: rs377603922
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876515G>A

(GRCh38)7:151877017C>G

(Homo sapiens)
Allele/Variant
Source: rs886062106
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151877017C>G

(GRCh38)7:151876543G>A

(Homo sapiens)
Allele/Variant
Source: NC_000007.14:g.151876543G>A
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876543G>A

(GRCh38)7:151876581C>G

(Homo sapiens)
Allele/Variant
Source: rs150188173
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876581C>G

(GRCh38)7:151876660G>A

(Homo sapiens)
Allele/Variant
Source: rs148715621
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876660G>A

(GRCh38)7:151877134C>A

(Homo sapiens)
Allele/Variant
Source: rs1007252189
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151877134C>A

(GRCh38)7:151876532C>T

(Homo sapiens)
Allele/Variant
Source: rs1338205156
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (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)7:151876532C>T

(GRCh38)7:151877140G>A

(Homo sapiens)
Allele/Variant
Source: rs73160072
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151877140G>A

(GRCh38)7:151876507C>G

(Homo sapiens)
Allele/Variant
Source: rs397517261
Genes: PRKAG2-AS1 (Hsa), PRKAG2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:151876507C>G