Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Genes
Allele/Variant
Actr8tm1.1(KOMP)Vlcg
(Mus musculus)Allele/Variant
Source: MGI:5554924
Genes: Actr8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Actr8
Genes: Actr8 (Mmu)
Symbol: Actr8tm1.1(KOMP)Vlcg
sa25411
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-12527
Genes: actr8 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_region_variant, stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: actr8 (Dre)
(GRCh38)3:53871420G>A
(Homo sapiens)Allele/Variant
Source: rs1030608705
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53871420G>A
(GRCh38)3:53876685T>C
(Homo sapiens)Allele/Variant
Source: rs758841076
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53876685T>C
(GRCh38)3:53871370G>C
(Homo sapiens)Allele/Variant
Source: rs769409988
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53871370G>C
(GRCh38)3:53877741T>G
(Homo sapiens)Allele/Variant
Source: rs899734209
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53877741T>G
(GRCh38)3:53877702G>A
(Homo sapiens)Allele/Variant
Source: rs780432704
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53877702G>A
(GRCh38)3:53879947C>T
(Homo sapiens)Allele/Variant
Source: rs928554394
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53879947C>T
(GRCh38)3:53868765C>T
(Homo sapiens)Allele/Variant
Source: rs761315684
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53868765C>T
(GRCh38)3:53876051C>T
(Homo sapiens)Allele/Variant
Source: rs749555757
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53876051C>T
(GRCh38)3:53872521G>A
(Homo sapiens)Allele/Variant
Source: rs371924812
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53872521G>A
(GRCh38)3:53876683T>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.53876683T>A
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53876683T>A
(GRCh38)3:53868727C>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.53868727C>T
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53868727C>T
(GRCh38)3:53871316T>C
(Homo sapiens)Allele/Variant
Source: rs373055423
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)3:53871316T>C
(GRCh38)3:53877744G>C
(Homo sapiens)Allele/Variant
Source: rs1208579176
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53877744G>C
(GRCh38)3:53878392T>C
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.53878392T>C
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53878392T>C
(GRCh38)3:53874236T>G
(Homo sapiens)Allele/Variant
Source: rs376401536
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53874236T>G
(GRCh38)3:53877377A>C
(Homo sapiens)Allele/Variant
Source: rs1273252274
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53877377A>C
(GRCh38)3:53868814A>C
(Homo sapiens)Allele/Variant
Source: rs1385458995
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53868814A>C
(GRCh38)3:53874273T>C
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.53874273T>C
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53874273T>C
(GRCh38)3:53878365G>C
(Homo sapiens)Allele/Variant
Source: rs1218703426
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53878365G>C
(GRCh38)3:53880003C>T
(Homo sapiens)Allele/Variant
Source: rs752053283
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53880003C>T
(GRCh38)3:53870044T>G
(Homo sapiens)Allele/Variant
Source: rs770170566
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53870044T>G
(GRCh38)3:53877711T>C
(Homo sapiens)Allele/Variant
Source: rs768886722
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53877711T>C
(GRCh38)3:53877747C>T
(Homo sapiens)Allele/Variant
Source: rs149202945
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53877747C>T
(GRCh38)3:53870100A>C
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.53870100A>C
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53870100A>C
(GRCh38)3:53872524C>A
(Homo sapiens)Allele/Variant
Source: rs201796393
Genes: ACTR8 (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)3:53872524C>A
(GRCh38)3:53877726C>T
(Homo sapiens)Allele/Variant
Source: rs1416966322
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53877726C>T
(GRCh38)3:53871366C>G
(Homo sapiens)Allele/Variant
Source: rs199775265
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53871366C>G
(GRCh38)3:53873105T>C
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.53873105T>C
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53873105T>C
(GRCh38)3:53876009C>T
(Homo sapiens)Allele/Variant
Source: rs752599288
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53876009C>T
(GRCh38)3:53877758A>C
(Homo sapiens)Allele/Variant
Source: rs201378833
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53877758A>C
(GRCh38)3:53872433T>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.53872433T>A
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53872433T>A
(GRCh38)3:53877688T>C
(Homo sapiens)Allele/Variant
Source: rs150103066
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53877688T>C
(GRCh38)3:53880031G>C
(Homo sapiens)Allele/Variant
Source: rs772847580
Genes: ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53880031G>C
(GRCh38)3:53864926T>C
(Homo sapiens)Allele/Variant
Source: rs377005084
Genes: IL17RB (Hsa), ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53864926T>C
(GRCh38)3:53860142C>T
(Homo sapiens)Allele/Variant
Source: rs750088430
Genes: IL17RB (Hsa), ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53860142C>T
(GRCh38)3:53864764C>T
(Homo sapiens)Allele/Variant
Source: rs563112234
Genes: IL17RB (Hsa), ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53864764C>T
(GRCh38)3:53864925A>G
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.53864925A>G
Genes: IL17RB (Hsa), ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53864925A>G
(GRCh38)3:53865143T>G
(Homo sapiens)Allele/Variant
Source: rs1341546454
Genes: IL17RB (Hsa), ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53865143T>G
(GRCh38)3:53865213G>A
(Homo sapiens)Allele/Variant
Source: rs1436249006
Genes: IL17RB (Hsa), ACTR8 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:53865213G>A
(mRatBN7.2)16:5170407G>T
(Rattus norvegicus)Allele/Variant
Source: rs3322686791
Genes: Actr8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:5170407G>T
(mRatBN7.2)16:5171038C>T
(Rattus norvegicus)Allele/Variant
Source: rs8172533
Genes: Actr8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:5171038C>T
(mRatBN7.2)16:5171132C>T
(Rattus norvegicus)Allele/Variant
Source: rs106357259
Genes: Actr8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:5171132C>T
(mRatBN7.2)16:5172106G>C
(Rattus norvegicus)Allele/Variant
Source: rs198475885
Genes: Actr8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:5172106G>C
(mRatBN7.2)16:5176518C>T
(Rattus norvegicus)Allele/Variant
Source: rs197819449
Genes: Actr8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:5176518C>T
(mRatBN7.2)16:5164974T>C
(Rattus norvegicus)Allele/Variant
Source: rs3322686681
Genes: Actr8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:5164974T>C
(mRatBN7.2)16:5169167C>T
(Rattus norvegicus)Allele/Variant
Source: rs3322503259
Genes: Actr8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:5169167C>T
(mRatBN7.2)16:5179635C>T
(Rattus norvegicus)Allele/Variant
Source: rs106500891
Genes: Actr8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:5179635C>T
(mRatBN7.2)16:5168914T>C
(Rattus norvegicus)Allele/Variant
Source: rs198262453
Genes: Actr8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:5168914T>C