Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CSF1 (Hsa)
(GRCh38)1:109924063A>T
(Homo sapiens)Allele/Variant
Source: rs749554501
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109924063A>T
(GRCh38)1:109911058C>G
(Homo sapiens)Allele/Variant
Source: rs987277680
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109911058C>G
(GRCh38)1:109917459A>C
(Homo sapiens)Allele/Variant
Source: rs987951166
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109917459A>C
(GRCh38)1:109923364G>A
(Homo sapiens)Allele/Variant
Source: rs750809815
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923364G>A
(GRCh38)1:109921866A>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.109921866A>G
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109921866A>G
(GRCh38)1:109923465C>A
(Homo sapiens)Allele/Variant
Source: rs147144390
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923465C>A
(GRCh38)1:109923921G>C
(Homo sapiens)Allele/Variant
Source: rs146089530
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923921G>C
(GRCh38)1:109923966C>T
(Homo sapiens)Allele/Variant
Source: rs369579772
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923966C>T
(GRCh38)1:109921853G>C
(Homo sapiens)Allele/Variant
Source: rs377085953
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109921853G>C
(GRCh38)1:109924783A>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.109924783A>G
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109924783A>G
(GRCh38)1:109911033C>T
(Homo sapiens)Allele/Variant
Source: rs779110244
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109911033C>T
(GRCh38)1:109923354G>C
(Homo sapiens)Allele/Variant
Source: rs369018338
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923354G>C
(GRCh38)1:109924798C>T
(Homo sapiens)Allele/Variant
Source: rs2229167
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109924798C>T
(GRCh38)1:109923913C>T
(Homo sapiens)Allele/Variant
Source: rs199818340
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923913C>T
(GRCh38)1:109923478C>A
(Homo sapiens)Allele/Variant
Source: rs777803639
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923478C>A
(GRCh38)1:109924154C>T
(Homo sapiens)Allele/Variant
Source: rs3208449
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109924154C>T
(GRCh38)1:109923833G>A
(Homo sapiens)Allele/Variant
Source: rs149423163
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923833G>A
(GRCh38)1:109923274T>G
(Homo sapiens)Allele/Variant
Source: rs267597915
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923274T>G
(GRCh38)1:109923497G>A
(Homo sapiens)Allele/Variant
Source: rs12721513
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923497G>A
(GRCh38)1:109923580G>T
(Homo sapiens)Allele/Variant
Source: rs199950075
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923580G>T
(GRCh38)1:109924105A>G
(Homo sapiens)Allele/Variant
Source: rs373422212
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109924105A>G
(GRCh38)1:109923910C>T
(Homo sapiens)Allele/Variant
Source: rs776875416
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923910C>T
(GRCh38)1:109921915A>C
(Homo sapiens)Allele/Variant
Source: rs759668151
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109921915A>C
(GRCh38)1:109923269C>T
(Homo sapiens)Allele/Variant
Source: rs267597914
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923269C>T
(GRCh38)1:109924039C>T
(Homo sapiens)Allele/Variant
Source: rs267597916
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109924039C>T
(GRCh38)1:109911030G>A
(Homo sapiens)Allele/Variant
Source: rs1654656504
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109911030G>A
(GRCh38)1:109923397A>G
(Homo sapiens)Allele/Variant
Source: rs752931255
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923397A>G
(GRCh38)1:109923447G>A
(Homo sapiens)Allele/Variant
Source: rs775031771
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923447G>A
(GRCh38)1:109923252C>T
(Homo sapiens)Allele/Variant
Source: rs149810852
Genes: CSF1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:109923252C>T