Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Diseases
Genes
Allele/Variant
zf3878
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-240814-2
Genes: odad2 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: armc4
Odad2em1(IMPC)Mbp
(Mus musculus)Allele/Variant
Source: MGI:6277027
Genes: Odad2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Armc4
sa42032
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-17199
Genes: odad2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: armc4
(GRCh38)10:27983938G>A
(Homo sapiens)Allele/Variant
Source: rs369669370
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983938G>A
Gene Synonyms: ARMC4
(GRCh38)10:27987521C>A
(Homo sapiens)Allele/Variant
Source: rs747965765
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27987521C>A
Gene Synonyms: ARMC4
(GRCh38)10:27985220A>T
(Homo sapiens)Allele/Variant
Source: rs1193786815
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27985220A>T
Gene Synonyms: ARMC4
(GRCh38)10:27860823A>C
(Homo sapiens)Allele/Variant
Source: rs575075615
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27860823A>C
Gene Synonyms: ARMC4
(GRCh38)10:27935219C>T
(Homo sapiens)Allele/Variant
Source: rs780112130
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27935219C>T
Gene Synonyms: ARMC4
(GRCh38)10:27971311T>C
(Homo sapiens)Allele/Variant
Source: rs766491818
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27971311T>C
Gene Synonyms: ARMC4
(GRCh38)10:27983859C>A
(Homo sapiens)Allele/Variant
Source: rs372616728
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983859C>A
Gene Synonyms: ARMC4
(GRCh38)10:27985060C>A
(Homo sapiens)Allele/Variant
Source: rs550542420
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27985060C>A
Gene Synonyms: ARMC4
(GRCh38)10:27987508T>C
(Homo sapiens)Allele/Variant
Source: rs1465895645
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27987508T>C
Gene Synonyms: ARMC4
(GRCh38)10:27984224T>C
(Homo sapiens)Allele/Variant
Source: rs1849734366
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27984224T>C
Gene Synonyms: ARMC4
(GRCh38)10:27936707A>T
(Homo sapiens)Allele/Variant
Source: rs2134099850
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27936707A>T
Gene Synonyms: ARMC4
(GRCh38)10:27983835T>G
(Homo sapiens)Allele/Variant
Source: rs1236480521
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983835T>G
Gene Synonyms: ARMC4
(GRCh38)10:27983882C>T
(Homo sapiens)Allele/Variant
Source: rs2133123588
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983882C>T
Gene Synonyms: ARMC4
(GRCh38)10:27983945C>T
(Homo sapiens)Allele/Variant
Source: rs150780082
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983945C>T
Gene Synonyms: ARMC4
(GRCh38)10:27984433A>C
(Homo sapiens)Allele/Variant
Source: rs55716902
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27984433A>C
Gene Synonyms: ARMC4
(GRCh38)10:27987616T>C
(Homo sapiens)Allele/Variant
Source: rs146689340
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27987616T>C
Gene Synonyms: ARMC4
(GRCh38)10:27994951C>T
(Homo sapiens)Allele/Variant
Source: rs760968744
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27994951C>T
Gene Synonyms: ARMC4
(GRCh38)10:27995046C>A
(Homo sapiens)Allele/Variant
Source: rs752348839
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, stop_gained
Diseases: Not Available
Variant Name: (GRCh38)10:27995046C>A
Gene Synonyms: ARMC4
(GRCh38)10:27860633C>T
(Homo sapiens)Allele/Variant
Source: rs1167723751
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27860633C>T
Gene Synonyms: ARMC4
(GRCh38)10:27860646C>T
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.27860646C>T
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27860646C>T
Gene Synonyms: ARMC4
(GRCh38)10:27812526C>A
(Homo sapiens)Allele/Variant
Source: rs3737184
Genes: ODAD2 (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)10:27812526C>A
Gene Synonyms: ARMC4
(GRCh38)10:27862558G>T
(Homo sapiens)Allele/Variant
Source: rs587777049
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27862558G>T
Gene Synonyms: ARMC4
(GRCh38)10:27862603C>T
(Homo sapiens)Allele/Variant
Source: rs376143899
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27862603C>T
Gene Synonyms: ARMC4
(GRCh38)10:27939983C>T
(Homo sapiens)Allele/Variant
Source: rs1060503678
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27939983C>T
Gene Synonyms: ARMC4
(GRCh38)10:27944889T>A
(Homo sapiens)Allele/Variant
Source: rs773452157
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944889T>A
Gene Synonyms: ARMC4
(GRCh38)10:27940580G>A
(Homo sapiens)Allele/Variant
Source: rs868755574
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27940580G>A
Gene Synonyms: ARMC4
(GRCh38)10:27944820C>T
(Homo sapiens)Allele/Variant
Source: rs1472984153
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944820C>T
Gene Synonyms: ARMC4
(GRCh38)10:27937154C>T
(Homo sapiens)Allele/Variant
Source: rs58502831
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27937154C>T
Gene Synonyms: ARMC4
(GRCh38)10:27971148C>G
(Homo sapiens)Allele/Variant
Source: rs775228185
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27971148C>G
Gene Synonyms: ARMC4
(GRCh38)10:27939877G>A
(Homo sapiens)Allele/Variant
Source: rs764297273
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27939877G>A
Gene Synonyms: ARMC4
(GRCh38)10:27860762G>A
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.27860762G>A
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27860762G>A
Gene Synonyms: ARMC4
(GRCh38)10:27940804A>T
(Homo sapiens)Allele/Variant
Source: rs1245635112
Genes: ODAD2 (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)10:27940804A>T
Gene Synonyms: ARMC4
(GRCh38)10:27936816C>T
(Homo sapiens)Allele/Variant
Source: rs762544821
Genes: ODAD2 (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)10:27936816C>T
Gene Synonyms: ARMC4
(GRCh38)10:27944966C>T
(Homo sapiens)Allele/Variant
Source: rs1590099355
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944966C>T
Gene Synonyms: ARMC4
(GRCh38)10:27907763A>G
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.27907763A>G
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27907763A>G
Gene Synonyms: ARMC4
(GRCh38)10:27961549T>C
(Homo sapiens)Allele/Variant
Source: rs1388906763
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27961549T>C
Gene Synonyms: ARMC4
(GRCh38)10:27944351T>C
(Homo sapiens)Allele/Variant
Source: rs920398574
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944351T>C
Gene Synonyms: ARMC4
(GRCh38)10:27961564T>C
(Homo sapiens)Allele/Variant
Source: rs199776339
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27961564T>C
Gene Synonyms: ARMC4
(GRCh38)10:27944373A>C
(Homo sapiens)Allele/Variant
Source: rs370164015
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944373A>C
Gene Synonyms: ARMC4
(GRCh38)10:27971274G>C
(Homo sapiens)Allele/Variant
Source: rs1032612529
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27971274G>C
Gene Synonyms: ARMC4
sa9510
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-130411-5127
Genes: odad2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: armc4
sa8644
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-19387
Genes: odad2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: armc4
(GRCh38)10:27987558T>C
(Homo sapiens)Allele/Variant
Source: rs1448669531
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27987558T>C
Gene Synonyms: ARMC4
(GRCh38)10:27995475T>C
(Homo sapiens)Allele/Variant
Source: rs4385792
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27995475T>C
Gene Synonyms: ARMC4
(GRCh38)10:27861079C>T
(Homo sapiens)Allele/Variant
Source: rs59540473
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27861079C>T
Gene Synonyms: ARMC4
(GRCh38)10:27984194T>C
(Homo sapiens)Allele/Variant
Source: rs1299728001
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27984194T>C
Gene Synonyms: ARMC4
(GRCh38)10:27987379A>G
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.27987379A>G
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27987379A>G
Gene Synonyms: ARMC4