Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Diseases
Genes
Construct Expressed Component
Construct Knockdown Component
Construct Regulatory Region
Allele/Variant
(R6)X:17149116A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149116A>T
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17149116A>T
Gene Synonyms: CHCHD2
(R6)X:17149588A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149588A>C
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149588A>C
Gene Synonyms: CHCHD2
(R6)X:17149275G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149275G>T
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149275G>T
Gene Synonyms: CHCHD2
(R6)X:17149069C>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149069C>G
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17149069C>G
Gene Synonyms: CHCHD2
(R6)X:17149084A>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149084A>G
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17149084A>G
Gene Synonyms: CHCHD2
(R6)X:17149481G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149481G>A
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149481G>A
Gene Synonyms: CHCHD2
(R6)X:17149508T>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149508T>C
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149508T>C
Gene Synonyms: CHCHD2
(R6)X:17149756A>C
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149756A>C
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149756A>C
Gene Synonyms: CHCHD2
(R6)X:17149858C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149858C>T
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17149858C>T
Gene Synonyms: CHCHD2
(R6)X:17149910T>G
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149910T>G
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17149910T>G
Gene Synonyms: CHCHD2
(R6)X:17150353G>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17150353G>T
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17150353G>T
Gene Synonyms: CHCHD2
(R6)X:17149372A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149372A>T
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149372A>T
Gene Synonyms: CHCHD2
(R6)X:17149029T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149029T>A
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17149029T>A
Gene Synonyms: CHCHD2
(R6)X:17149242G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149242G>A
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149242G>A
Gene Synonyms: CHCHD2
(R6)X:17149522_17149524delinsC
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149522_17149524delinsC
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: delins
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149522_17149524delinsC
Gene Synonyms: CHCHD2
(R6)X:17149549A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149549A>T
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149549A>T
Gene Synonyms: CHCHD2
(R6)X:17149604T>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149604T>A
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149604T>A
Gene Synonyms: CHCHD2
(R6)X:17149700A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149700A>T
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149700A>T
Gene Synonyms: CHCHD2
(R6)X:17149755C>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17149755C>T
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17149755C>T
Gene Synonyms: CHCHD2
(R6)X:17150281G>A
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17150281G>A
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17150281G>A
Gene Synonyms: CHCHD2
(R6)X:17150521A>T
(Drosophila melanogaster)Allele/Variant
Source: NC_004354.4:g.17150521A>T
Genes: Chchd2 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17150521A>T
Gene Synonyms: CHCHD2
sa35803
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-4149
Genes: chchd2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_acceptor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: chchd2 (Dre)
sa18461
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-131217-14472
Genes: chchd10 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: chchd2
(GRCh38)7:56104379C>A
(Homo sapiens)Allele/Variant
Source: rs779261129
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104379C>A
(GRCh38)7:56104401G>A
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.56104401G>A
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104401G>A
(GRCh38)7:56104451T>G
(Homo sapiens)Allele/Variant
Source: rs941014757
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104451T>G
(GRCh38)7:56104242G>A
(Homo sapiens)Allele/Variant
Source: rs751030096
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104242G>A
(GRCh38)7:56106404C>T
(Homo sapiens)Allele/Variant
Source: rs778328496
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56106404C>T
(GRCh38)7:56104292G>A
(Homo sapiens)Allele/Variant
Source: rs143197896
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104292G>A
(GRCh38)7:56104344G>A
(Homo sapiens)Allele/Variant
Source: rs864309650
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104344G>A
(GRCh38)7:56104411G>T
(Homo sapiens)Allele/Variant
Source: rs762109397
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104411G>T
(GRCh38)7:56104448G>A
(Homo sapiens)Allele/Variant
Source: rs753881759
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104448G>A
(GRCh38)7:56102907C>A
(Homo sapiens)Allele/Variant
Source: rs775396143
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56102907C>A
(GRCh38)7:56104375G>A
(Homo sapiens)Allele/Variant
Source: rs757126911
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104375G>A
(GRCh38)7:56104432C>G
(Homo sapiens)Allele/Variant
Source: rs145190179
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104432C>G
(GRCh38)7:56104432C>T
(Homo sapiens)Allele/Variant
Source: rs145190179
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104432C>T
(GRCh38)7:56104461A>G
(Homo sapiens)Allele/Variant
Source: rs757118379
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104461A>G
(GRCh38)7:56102953T>C
(Homo sapiens)Allele/Variant
Source: rs1364264066
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56102953T>C
(GRCh38)7:56104219T>G
(Homo sapiens)Allele/Variant
Source: rs764589776
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104219T>G
(GRCh38)7:56104262A>G
(Homo sapiens)Allele/Variant
Source: rs1785340599
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104262A>G
(GRCh38)7:56104221C>T
(Homo sapiens)Allele/Variant
Source: rs750014782
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104221C>T
(GRCh38)7:56106260G>T
(Homo sapiens)Allele/Variant
Source: rs190266344
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56106260G>T
(GRCh38)7:56104425G>A
(Homo sapiens)Allele/Variant
Source: rs371198317
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104425G>A
(GRCh38)7:56106447G>T
(Homo sapiens)Allele/Variant
Source: rs816407
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56106447G>T
(GRCh38)7:56106123A>G
(Homo sapiens)Allele/Variant
Source: rs6971804
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56106123A>G
(GRCh38)7:56106382C>T
(Homo sapiens)Allele/Variant
Source: rs373956381
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56106382C>T
(GRCh38)7:56102951A>C
(Homo sapiens)Allele/Variant
Source: rs1785316360
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56102951A>C
(GRCh38)7:56101726C>T
(Homo sapiens)Allele/Variant
Source: rs8406
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56101726C>T
(GRCh38)7:56102853G>A
(Homo sapiens)Allele/Variant
Source: rs201421064
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56102853G>A
(GRCh38)7:56104233G>A
(Homo sapiens)Allele/Variant
Source: rs2115579934
Genes: CHCHD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:56104233G>A