Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Cfpem1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7296888
Genes: Cfp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Pfc
Cfptm1.1Song
(Mus musculus)Allele/Variant
Source: MGI:3771611
Genes: Cfp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Pfc
Cfpem1Smoc
(Mus musculus)Allele/Variant
Source: MGI:7288948
Genes: Cfp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Pfc
Cfptm1Song
(Mus musculus)Allele/Variant
Source: MGI:3771610
Genes: Cfp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Pfc
Cfptm2.1Song
(Mus musculus)Allele/Variant
Source: MGI:4838300
Genes: Cfp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Pfc
Cfptm1Cmst
(Mus musculus)Allele/Variant
Source: MGI:3774548
Genes: Cfp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Pfc
Cfpem1(IMPC)H
(Mus musculus)Allele/Variant
Source: MGI:7425583
Genes: Cfp (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Pfc
(GRCh38)X:47627296G>A
(Homo sapiens)Allele/Variant
Source: rs8177076
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627296G>A
Gene Synonyms: PFC
(GRCh38)X:47627618C>T
(Homo sapiens)Allele/Variant
Source: rs1190480861
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627618C>T
Gene Synonyms: PFC
(GRCh38)X:47629630C>T
(Homo sapiens)Allele/Variant
Source: rs374687577
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629630C>T
Gene Synonyms: PFC
(GRCh38)X:47627191G>A
(Homo sapiens)Allele/Variant
Source: rs200036265
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627191G>A
Gene Synonyms: PFC
(GRCh38)X:47629677G>A
(Homo sapiens)Allele/Variant
Source: rs918926806
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629677G>A
Gene Synonyms: PFC
(GRCh38)X:47629803C>T
(Homo sapiens)Allele/Variant
Source: rs371398463
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629803C>T
Gene Synonyms: PFC
(GRCh38)X:47629827C>T
(Homo sapiens)Allele/Variant
Source: rs1020912849
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629827C>T
Gene Synonyms: PFC
(GRCh38)X:47624353C>T
(Homo sapiens)Allele/Variant
Source: rs141133000
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47624353C>T
Gene Synonyms: PFC
(GRCh38)X:47626066G>A
(Homo sapiens)Allele/Variant
Source: rs774205180
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626066G>A
Gene Synonyms: PFC
(GRCh38)X:47626309C>G
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.47626309C>G
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626309C>G
Gene Synonyms: PFC
(GRCh38)X:47626343T>C
(Homo sapiens)Allele/Variant
Source: rs935700885
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626343T>C
Gene Synonyms: PFC
(GRCh38)X:47627576G>A
(Homo sapiens)Allele/Variant
Source: rs745424947
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627576G>A
Gene Synonyms: PFC
(GRCh38)X:47627580C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.47627580C>T
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627580C>T
Gene Synonyms: PFC
(GRCh38)X:47627634G>A
(Homo sapiens)Allele/Variant
Source: rs1202037341
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627634G>A
Gene Synonyms: PFC
(GRCh38)X:47628093C>T
(Homo sapiens)Allele/Variant
Source: rs8177075
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47628093C>T
Gene Synonyms: PFC
(GRCh38)X:47629551C>T
(Homo sapiens)Allele/Variant
Source: rs370592348
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629551C>T
Gene Synonyms: PFC
(GRCh38)X:47626804G>A
(Homo sapiens)Allele/Variant
Source: rs757743217
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626804G>A
Gene Synonyms: PFC
(GRCh38)X:47626820C>A
(Homo sapiens)Allele/Variant
Source: rs28935480
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626820C>A
Gene Synonyms: PFC
(GRCh38)X:47627327C>T
(Homo sapiens)Allele/Variant
Source: rs755651023
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627327C>T
Gene Synonyms: PFC
(GRCh38)X:47628269C>T
(Homo sapiens)Allele/Variant
Source: rs761962858
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47628269C>T
Gene Synonyms: PFC
(GRCh38)X:47626501G>A
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.47626501G>A
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626501G>A
Gene Synonyms: PFC
(GRCh38)X:47624356T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.47624356T>C
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47624356T>C
Gene Synonyms: PFC
(GRCh38)X:47626115C>T
(Homo sapiens)Allele/Variant
Source: rs1167161113
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626115C>T
Gene Synonyms: PFC
(GRCh38)X:47626122G>A
(Homo sapiens)Allele/Variant
Source: rs756946812
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626122G>A
Gene Synonyms: PFC
(GRCh38)X:47627295G>A
(Homo sapiens)Allele/Variant
Source: rs1031008836
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627295G>A
Gene Synonyms: PFC
(GRCh38)X:47627564G>A
(Homo sapiens)Allele/Variant
Source: rs132630258
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627564G>A
Gene Synonyms: PFC
(GRCh38)X:47629610C>G
(Homo sapiens)Allele/Variant
Source: rs759507756
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629610C>G
Gene Synonyms: PFC
(GRCh38)X:47627633C>T
(Homo sapiens)Allele/Variant
Source: rs771566525
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627633C>T
Gene Synonyms: PFC
(GRCh38)X:47628082G>A
(Homo sapiens)Allele/Variant
Source: rs1383306170
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47628082G>A
Gene Synonyms: PFC
(GRCh38)X:47626411C>T
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.47626411C>T
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626411C>T
Gene Synonyms: PFC
(GRCh38)X:47626498C>A
(Homo sapiens)Allele/Variant
Source: rs778252094
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626498C>A
Gene Synonyms: PFC
(GRCh38)X:47626097G>C
(Homo sapiens)Allele/Variant
Source: rs757339568
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626097G>C
Gene Synonyms: PFC
(GRCh38)X:47626865G>A
(Homo sapiens)Allele/Variant
Source: rs1325258357
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47626865G>A
Gene Synonyms: PFC
(GRCh38)X:47627159C>T
(Homo sapiens)Allele/Variant
Source: rs8177077
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627159C>T
Gene Synonyms: PFC
(GRCh38)X:47628200C>T
(Homo sapiens)Allele/Variant
Source: rs2147937441
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47628200C>T
Gene Synonyms: PFC
(GRCh38)X:47628288G>A
(Homo sapiens)Allele/Variant
Source: rs1380731149
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47628288G>A
Gene Synonyms: PFC
(GRCh38)X:47629506C>G
(Homo sapiens)Allele/Variant
Source: rs769946055
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629506C>G
Gene Synonyms: PFC
(GRCh38)X:47629514T>G
(Homo sapiens)Allele/Variant
Source: rs1447794687
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629514T>G
Gene Synonyms: PFC
(GRCh38)X:47629522A>C
(Homo sapiens)Allele/Variant
Source: rs1317275240
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629522A>C
Gene Synonyms: PFC
(GRCh38)X:47629664G>A
(Homo sapiens)Allele/Variant
Source: rs747543016
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47629664G>A
Gene Synonyms: PFC
(GRCh38)X:47627325C>A
(Homo sapiens)Allele/Variant
Source: rs781475195
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627325C>A
Gene Synonyms: PFC
(GRCh38)X:47627573T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.47627573T>C
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627573T>C
Gene Synonyms: PFC
(GRCh38)X:47627584T>C
(Homo sapiens)Allele/Variant
Source: NC_000023.11:g.47627584T>C
Genes: CFP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)X:47627584T>C
Gene Synonyms: PFC