Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CSF1R (Hsa)
(GRCh38)5:150086752C>G
(Homo sapiens)Allele/Variant
Source: rs73275678
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150086752C>G
(GRCh38)5:150113329C>T
(Homo sapiens)Allele/Variant
Source: rs180988739
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150113329C>T
(GRCh38)5:150054326T>G
(Homo sapiens)Allele/Variant
Source: rs964312276
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054326T>G
(GRCh38)5:150054429A>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.150054429A>G
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054429A>G
(GRCh38)5:150054182C>T
(Homo sapiens)Allele/Variant
Source: rs537011691
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054182C>T
(GRCh38)5:150055288A>C
(Homo sapiens)Allele/Variant
Source: rs281860278
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150055288A>C
(GRCh38)5:150054294C>G
(Homo sapiens)Allele/Variant
Source: rs41533349
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054294C>G
(GRCh38)5:150054315C>T
(Homo sapiens)Allele/Variant
Source: rs371729310
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054315C>T
(GRCh38)5:150056053T>A
(Homo sapiens)Allele/Variant
Source: rs690016558
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150056053T>A
(GRCh38)5:150053538G>A
(Homo sapiens)Allele/Variant
Source: rs367836988
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150053538G>A
(GRCh38)5:150113280G>A
(Homo sapiens)Allele/Variant
Source: rs1282627420
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150113280G>A
(GRCh38)5:150054327C>T
(Homo sapiens)Allele/Variant
Source: rs200925061
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054327C>T
(GRCh38)5:150054102G>A
(Homo sapiens)Allele/Variant
Source: rs370648666
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054102G>A
(GRCh38)5:150054103G>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.150054103G>A
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054103G>A
(GRCh38)5:150054122G>A
(Homo sapiens)Allele/Variant
Source: rs2113772523
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054122G>A
(GRCh38)5:150054210C>T
(Homo sapiens)Allele/Variant
Source: rs1757075635
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054210C>T
(GRCh38)5:150054313C>T
(Homo sapiens)Allele/Variant
Source: rs747191440
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054313C>T
(GRCh38)5:150054323C>G
(Homo sapiens)Allele/Variant
Source: rs56059682
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054323C>G
(GRCh38)5:150053530G>T
(Homo sapiens)Allele/Variant
Source: rs373206666
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150053530G>T
(GRCh38)5:150053759G>T
(Homo sapiens)Allele/Variant
Source: rs41497048
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150053759G>T
(GRCh38)5:150054083A>G
(Homo sapiens)Allele/Variant
Source: rs121913393
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054083A>G
(GRCh38)5:150054159C>T
(Homo sapiens)Allele/Variant
Source: rs769701747
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054159C>T
(GRCh38)5:150054206T>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.150054206T>C
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150054206T>C
(GRCh38)5:150053664C>G
(Homo sapiens)Allele/Variant
Source: rs1058920
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150053664C>G
(GRCh38)5:150055262G>A
(Homo sapiens)Allele/Variant
Source: rs690016556
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150055262G>A
(GRCh38)5:150055334G>A
(Homo sapiens)Allele/Variant
Source: rs372774226
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150055334G>A
(GRCh38)5:150056035A>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.150056035A>C
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150056035A>C
(GRCh38)5:150056039C>G
(Homo sapiens)Allele/Variant
Source: rs690016551
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150056039C>G
(GRCh38)5:150053295T>C
(Homo sapiens)Allele/Variant
Source: rs371174880
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150053295T>C
(GRCh38)5:150053450C>A
(Homo sapiens)Allele/Variant
Source: rs1757015333
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150053450C>A
(GRCh38)5:150060680G>A
(Homo sapiens)Allele/Variant
Source: rs10061550
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150060680G>A
(GRCh38)5:150060873C>T
(Homo sapiens)Allele/Variant
Source: rs397515555
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150060873C>T
(GRCh38)5:150056319G>T
(Homo sapiens)Allele/Variant
Source: rs587777247
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150056319G>T
(GRCh38)5:150061762T>C
(Homo sapiens)Allele/Variant
Source: rs1234517590
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150061762T>C
(GRCh38)5:150061772C>T
(Homo sapiens)Allele/Variant
Source: rs771243135
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150061772C>T
(GRCh38)5:150061775C>T
(Homo sapiens)Allele/Variant
Source: rs567201624
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150061775C>T
(GRCh38)5:150061776G>A
(Homo sapiens)Allele/Variant
Source: rs41529644
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150061776G>A
(GRCh38)5:150057343G>A
(Homo sapiens)Allele/Variant
Source: rs753256015
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150057343G>A
(GRCh38)5:150068338G>T
(Homo sapiens)Allele/Variant
Source: rs771138400
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150068338G>T
(GRCh38)5:150069856C>T
(Homo sapiens)Allele/Variant
Source: rs112616479
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150069856C>T
(GRCh38)5:150053968A>G
(Homo sapiens)Allele/Variant
Source: rs1757050261
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150053968A>G
(GRCh38)5:150059704G>A
(Homo sapiens)Allele/Variant
Source: rs762329575
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150059704G>A
(GRCh38)5:150059750C>T
(Homo sapiens)Allele/Variant
Source: rs56316417
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150059750C>T
(GRCh38)5:150059764C>T
(Homo sapiens)Allele/Variant
Source: rs141866247
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150059764C>T
(GRCh38)5:150059882G>A
(Homo sapiens)Allele/Variant
Source: rs767767475
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150059882G>A
(GRCh38)5:150057349G>A
(Homo sapiens)Allele/Variant
Source: rs372068592
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150057349G>A
(GRCh38)5:150057361G>A
(Homo sapiens)Allele/Variant
Source: rs373083937
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150057361G>A
(GRCh38)5:150060959A>C
(Homo sapiens)Allele/Variant
Source: rs139845496
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150060959A>C
(GRCh38)5:150061554C>G
(Homo sapiens)Allele/Variant
Source: rs2113792005
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150061554C>G
(GRCh38)5:150061585G>A
(Homo sapiens)Allele/Variant
Source: rs149436601
Genes: CSF1R (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:150061585G>A