Version: 8.1.0
Date: Fri Apr 18 2025
62 results for ATP2A1-AS1

ATP2A1-AS1

(Homo sapiens)
Gene
Name: ATP2A1 antisense RNA 1
Synonyms: Not Available
Source: HGNC:51370
Biotype: ncRNA gene
Symbol: ATP2A1-AS1 (Hsa)
Symbol: ATP2A1-AS1

(GRCh38)16:28878165C>A

(Homo sapiens)
Allele/Variant
Source: rs3888190
Genes: ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878165C>A

(GRCh38)16:28878729G>A

(Homo sapiens)
Allele/Variant
Source: rs1027940672
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878729G>A

(GRCh38)16:28878789G>A

(Homo sapiens)
Allele/Variant
Source: rs762501478
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878789G>A

(GRCh38)16:28878810C>A

(Homo sapiens)
Allele/Variant
Source: rs62037371
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878810C>A

(GRCh38)16:28879109T>C

(Homo sapiens)
Allele/Variant
Source: rs750655997
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879109T>C

(GRCh38)16:28878672A>G

(Homo sapiens)
Allele/Variant
Source: rs368689264
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, start_lost
Diseases: Not Available
Variant Name: (GRCh38)16:28878672A>G

(GRCh38)16:28879584G>C

(Homo sapiens)
Allele/Variant
Source: rs1963393226
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879584G>C

(GRCh38)16:28878650C>T

(Homo sapiens)
Allele/Variant
Source: rs75273069
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878650C>T

(GRCh38)16:28878657C>T

(Homo sapiens)
Allele/Variant
Source: rs761455664
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878657C>T

(GRCh38)16:28878785C>T

(Homo sapiens)
Allele/Variant
Source: rs1057522341
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878785C>T

(GRCh38)16:28878763G>A

(Homo sapiens)
Allele/Variant
Source: rs1596658318
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878763G>A

(GRCh38)16:28878759A>C

(Homo sapiens)
Allele/Variant
Source: rs777070879
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878759A>C

(GRCh38)16:28879108C>T

(Homo sapiens)
Allele/Variant
Source: rs150403167
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879108C>T

(GRCh38)16:28878787A>G

(Homo sapiens)
Allele/Variant
Source: rs2152195750
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878787A>G

(GRCh38)16:28879508C>G

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.28879508C>G
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879508C>G

(GRCh38)16:28879559C>A

(Homo sapiens)
Allele/Variant
Source: rs1555514587
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879559C>A

(GRCh38)16:28879565G>A

(Homo sapiens)
Allele/Variant
Source: rs1459156708
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879565G>A

(GRCh38)16:28879083T>C

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.28879083T>C
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879083T>C

(GRCh38)16:28878680C>T

(Homo sapiens)
Allele/Variant
Source: rs1021452481
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878680C>T

(GRCh38)16:28878771G>T

(Homo sapiens)
Allele/Variant
Source: rs141559558
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878771G>T

(GRCh38)16:28878790G>A

(Homo sapiens)
Allele/Variant
Source: rs992119026
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878790G>A

(GRCh38)16:28878665G>A

(Homo sapiens)
Allele/Variant
Source: rs1555514404
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878665G>A

(GRCh38)16:28879562C>G

(Homo sapiens)
Allele/Variant
Source: rs2152196860
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879562C>G

(GRCh38)16:28879562C>T

(Homo sapiens)
Allele/Variant
Source: rs2152196860
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879562C>T

(GRCh38)16:28879571A>C

(Homo sapiens)
Allele/Variant
Source: rs767648658
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879571A>C

(GRCh38)16:28878715A>G

(Homo sapiens)
Allele/Variant
Source: rs371085493
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878715A>G

(GRCh38)16:28878726A>G

(Homo sapiens)
Allele/Variant
Source: rs1963351388
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878726A>G

(GRCh38)16:28879514G>A

(Homo sapiens)
Allele/Variant
Source: rs756940046
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879514G>A

(GRCh38)16:28878660G>A

(Homo sapiens)
Allele/Variant
Source: rs201334168
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878660G>A

(GRCh38)16:28878790G>T

(Homo sapiens)
Allele/Variant
Source: rs992119026
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878790G>T

(GRCh38)16:28879490T>C

(Homo sapiens)
Allele/Variant
Source: rs1384007427
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879490T>C

(GRCh38)16:28879549T>G

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.28879549T>G
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879549T>G

(GRCh38)16:28879559C>T

(Homo sapiens)
Allele/Variant
Source: rs1555514587
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879559C>T

(GRCh38)16:28879564T>G

(Homo sapiens)
Allele/Variant
Source: rs2152196866
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879564T>G

(GRCh38)16:28879482C>T

(Homo sapiens)
Allele/Variant
Source: rs776235380
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879482C>T

(GRCh38)16:28879496C>G

(Homo sapiens)
Allele/Variant
Source: rs767974799
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879496C>G

(GRCh38)16:28879503A>G

(Homo sapiens)
Allele/Variant
Source: rs2152196778
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879503A>G

(GRCh38)16:28879136G>A

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.28879136G>A
Genes: ATP2A1 (Hsa), ATP2A1-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)16:28879136G>A

(GRCh38)16:28879222C>G

(Homo sapiens)
Allele/Variant
Source: rs80127885
Genes: ATP2A1 (Hsa), ATP2A1-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)16:28879222C>G

(GRCh38)16:28879487G>C

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.28879487G>C
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879487G>C

(GRCh38)16:28879572T>C

(Homo sapiens)
Allele/Variant
Source: rs752669373
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879572T>C

(GRCh38)16:28878677G>A

(Homo sapiens)
Allele/Variant
Source: rs1315772334
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878677G>A

(GRCh38)16:28878712C>A

(Homo sapiens)
Allele/Variant
Source: rs1320892017
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878712C>A

(GRCh38)16:28879568C>T

(Homo sapiens)
Allele/Variant
Source: rs1555514590
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (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)16:28879568C>T

(GRCh38)16:28879491C>T

(Homo sapiens)
Allele/Variant
Source: rs763292322
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28879491C>T

(GRCh38)16:28878737G>A

(Homo sapiens)
Allele/Variant
Source: rs780688111
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878737G>A

(GRCh38)16:28878675G>A

(Homo sapiens)
Allele/Variant
Source: NC_000016.10:g.28878675G>A
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878675G>A

(GRCh38)16:28878769T>A

(Homo sapiens)
Allele/Variant
Source: rs1409431511
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878769T>A

(GRCh38)16:28878749G>A

(Homo sapiens)
Allele/Variant
Source: rs886051878
Genes: ATP2A1 (Hsa), ATP2A1-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:28878749G>A