Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: DNAJC6 (Hsa)
(GRCh38)1:65366107C>T
(Homo sapiens)Allele/Variant
Source: rs864622011
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65366107C>T
(GRCh38)1:65366206T>G
(Homo sapiens)Allele/Variant
Source: rs748757918
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65366206T>G
(GRCh38)1:65385720G>A
(Homo sapiens)Allele/Variant
Source: rs1645865223
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65385720G>A
(GRCh38)1:65398818A>G
(Homo sapiens)Allele/Variant
Source: rs145175543
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65398818A>G
(GRCh38)1:65389371C>T
(Homo sapiens)Allele/Variant
Source: rs767476436
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65389371C>T
(GRCh38)1:65401836G>A
(Homo sapiens)Allele/Variant
Source: rs4915691
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65401836G>A
(GRCh38)1:65406073G>T
(Homo sapiens)Allele/Variant
Source: rs773670078
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65406073G>T
(GRCh38)1:65402191G>C
(Homo sapiens)Allele/Variant
Source: rs74081637
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65402191G>C
(GRCh38)1:65405867T>C
(Homo sapiens)Allele/Variant
Source: rs753885398
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65405867T>C
(GRCh38)1:65395018C>T
(Homo sapiens)Allele/Variant
Source: rs769067430
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65395018C>T
(GRCh38)1:65394977T>C
(Homo sapiens)Allele/Variant
Source: rs12077111
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65394977T>C
(GRCh38)1:65405973C>T
(Homo sapiens)Allele/Variant
Source: rs370155769
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65405973C>T
(GRCh38)1:65411188G>A
(Homo sapiens)Allele/Variant
Source: rs536427726
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65411188G>A
(GRCh38)1:65413199C>T
(Homo sapiens)Allele/Variant
Source: rs9436293
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65413199C>T
(GRCh38)1:65398892G>T
(Homo sapiens)Allele/Variant
Source: rs142342080
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65398892G>T
(GRCh38)1:65406015G>A
(Homo sapiens)Allele/Variant
Source: rs372625439
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65406015G>A
(GRCh38)1:65392678G>A
(Homo sapiens)Allele/Variant
Source: rs201766287
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65392678G>A
(GRCh38)1:65395004A>C
(Homo sapiens)Allele/Variant
Source: rs4582839
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65395004A>C
(GRCh38)1:65364622T>G
(Homo sapiens)Allele/Variant
Source: rs765899995
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65364622T>G
(GRCh38)1:65385808C>G
(Homo sapiens)Allele/Variant
Source: rs371261372
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65385808C>G
(GRCh38)1:65398537G>T
(Homo sapiens)Allele/Variant
Source: rs10889548
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65398537G>T
(GRCh38)1:65401812C>T
(Homo sapiens)Allele/Variant
Source: rs143504255
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65401812C>T
(GRCh38)1:65406052C>T
(Homo sapiens)Allele/Variant
Source: rs398122405
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65406052C>T
(GRCh38)1:65406336A>G
(Homo sapiens)Allele/Variant
Source: rs35980819
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65406336A>G
(GRCh38)1:65408354T>C
(Homo sapiens)Allele/Variant
Source: rs3818513
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65408354T>C
(GRCh38)1:65408675A>G
(Homo sapiens)Allele/Variant
Source: rs753691766
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65408675A>G
(GRCh38)1:65392594G>A
(Homo sapiens)Allele/Variant
Source: rs749160546
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65392594G>A
(GRCh38)1:65395019G>A
(Homo sapiens)Allele/Variant
Source: rs185245369
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65395019G>A
(GRCh38)1:65395035A>G
(Homo sapiens)Allele/Variant
Source: rs961974767
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65395035A>G
(GRCh38)1:65402032C>T
(Homo sapiens)Allele/Variant
Source: rs4915692
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65402032C>T
(GRCh38)1:65366050A>T
(Homo sapiens)Allele/Variant
Source: rs61757223
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)1:65366050A>T
(GRCh38)1:65386627A>G
(Homo sapiens)Allele/Variant
Source: rs11208643
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65386627A>G
(GRCh38)1:65392856G>C
(Homo sapiens)Allele/Variant
Source: rs1312034761
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65392856G>C
(GRCh38)1:65392643G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.65392643G>A
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65392643G>A
(GRCh38)1:65392677C>T
(Homo sapiens)Allele/Variant
Source: rs141779215
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65392677C>T
(GRCh38)1:65392833C>T
(Homo sapiens)Allele/Variant
Source: rs1553147125
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65392833C>T
(GRCh38)1:65309899C>G
(Homo sapiens)Allele/Variant
Source: rs547312338
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65309899C>G
(GRCh38)1:65351546G>C
(Homo sapiens)Allele/Variant
Source: rs207460154
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65351546G>C
(GRCh38)1:65405993C>T
(Homo sapiens)Allele/Variant
Source: rs935798985
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65405993C>T
(GRCh38)1:65379763A>C
(Homo sapiens)Allele/Variant
Source: rs1408994
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65379763A>C
(GRCh38)1:65395019G>T
(Homo sapiens)Allele/Variant
Source: rs185245369
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65395019G>T
(GRCh38)1:65411414G>A
(Homo sapiens)Allele/Variant
Source: rs764156036
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65411414G>A
(GRCh38)1:65389247C>G
(Homo sapiens)Allele/Variant
Source: rs370864885
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65389247C>G
(GRCh38)1:65379812A>C
(Homo sapiens)Allele/Variant
Source: rs74082626
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65379812A>C
(GRCh38)1:65406105C>T
(Homo sapiens)Allele/Variant
Source: rs193114909
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65406105C>T
(GRCh38)1:65394886A>G
(Homo sapiens)Allele/Variant
Source: rs774888599
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65394886A>G
(GRCh38)1:65398515A>G
(Homo sapiens)Allele/Variant
Source: rs10889547
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65398515A>G
(GRCh38)1:65411312C>T
(Homo sapiens)Allele/Variant
Source: rs149097758
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65411312C>T
(GRCh38)1:65398884A>G
(Homo sapiens)Allele/Variant
Source: rs371583880
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65398884A>G
(GRCh38)1:65401783G>A
(Homo sapiens)Allele/Variant
Source: rs1297943839
Genes: DNAJC6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:65401783G>A