Version: 8.0.0
Date: Tue Jan 28 2025
1,064 results for ccdc63

(GRCh38)12:110853485G>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.110853485G>C
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110853485G>C

(GRCh38)12:110898985G>C

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.110898985G>C
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110898985G>C

(GRCh38)12:110853547G>A

(Homo sapiens)
Allele/Variant
Source: rs1029847714
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110853547G>A

(GRCh38)12:110884104C>A

(Homo sapiens)
Allele/Variant
Source: rs151096735
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110884104C>A

(GRCh38)12:110880035A>G

(Homo sapiens)
Allele/Variant
Source: rs147414240
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110880035A>G

(GRCh38)12:110880045T>A

(Homo sapiens)
Allele/Variant
Source: rs376720183
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110880045T>A

(GRCh38)12:110884243G>A

(Homo sapiens)
Allele/Variant
Source: rs267603306
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110884243G>A

(mRatBN7.2)12:34435054G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322222022
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34435054G>A

(mRatBN7.2)12:34436884A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322072977
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34436884A>G

(mRatBN7.2)12:34437852C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322177052
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34437852C>T

(mRatBN7.2)12:34445509T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322030819
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34445509T>C

(mRatBN7.2)12:34446201G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.34446201G>A
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34446201G>A

(mRatBN7.2)12:34452081C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106772541
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34452081C>T

(mRatBN7.2)12:34453033C>T

(Rattus norvegicus)
Allele/Variant
Source: rs8171862
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34453033C>T

(mRatBN7.2)12:34452123C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322221893
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34452123C>T

(mRatBN7.2)12:34452670A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322072950
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34452670A>G

(mRatBN7.2)12:34452171A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106352658
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34452171A>G

(mRatBN7.2)12:34434479A>C

(Rattus norvegicus)
Allele/Variant
Source: rs107503913
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34434479A>C

(mRatBN7.2)12:34437851A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322267208
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34437851A>T

(mRatBN7.2)12:34438026G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105433327
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34438026G>A

(mRatBN7.2)12:34443281A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321877503
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34443281A>G

(mRatBN7.2)12:34447279G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322072925
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34447279G>T

(mRatBN7.2)12:34445601T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321877538
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34445601T>C

rs199025153

(Rattus norvegicus)
Allele/Variant
Source: rs199025153
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(mRatBN7.2)12:34426714C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322226402
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34426714C>A

(mRatBN7.2)12:34432782A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106389185
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34432782A>G

(mRatBN7.2)12:34431995A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.34431995A>G
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34431995A>G

(mRatBN7.2)12:34437603A>C

(Rattus norvegicus)
Allele/Variant
Source: rs105919627
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34437603A>C

(mRatBN7.2)12:34442538G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.34442538G>A
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34442538G>A

(mRatBN7.2)12:34442559A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.34442559A>G
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34442559A>G

(mRatBN7.2)12:34447835C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322226451
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34447835C>T

(mRatBN7.2)12:34437744C>T

(Rattus norvegicus)
Allele/Variant
Source: rs107546519
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34437744C>T

(mRatBN7.2)12:34438133T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322180464
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34438133T>G

(mRatBN7.2)12:34442483T>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.34442483T>G
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34442483T>G

(mRatBN7.2)12:34442562G>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.34442562G>T
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34442562G>T

(mRatBN7.2)12:34449461C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322177004
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34449461C>T

(mRatBN7.2)12:34430023C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322231092
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34430023C>A

(mRatBN7.2)12:34428582A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106748424
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34428582A>G

(mRatBN7.2)12:34451194A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322222011
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34451194A>G

(mRatBN7.2)12:34451563C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.34451563C>T
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34451563C>T

(mRatBN7.2)12:34427996T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106770110
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34427996T>C

(mRatBN7.2)12:34431115C>G

(Rattus norvegicus)
Allele/Variant
Source: rs106138086
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34431115C>G

(mRatBN7.2)12:34432084A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322238987
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34432084A>C

(mRatBN7.2)12:34442560G>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.34442560G>T
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34442560G>T

(mRatBN7.2)12:34450135G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322176882
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34450135G>T

(mRatBN7.2)12:34451925T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322030748
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34451925T>A

(mRatBN7.2)12:34448637G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322073002
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34448637G>A

(mRatBN7.2)12:34430591A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322030808
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34430591A>T

(mRatBN7.2)12:34429301A>C

(Rattus norvegicus)
Allele/Variant
Source: rs105004661
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34429301A>C

(mRatBN7.2)12:34431966C>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.34431966C>G
Genes: Ccdc63 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:34431966C>G