Version: 8.0.0
Date: Tue Jan 28 2025
rs112616479
Variant overlaps CSF1R
Homo sapiens
SummaryVariant Molecular Consequences
Allele/Variant

rs112616479

Species
Homo sapiens
Symbol
rs112616479
Category
Variant
Variant type
SNP
Overlaps
CSF1R
Location
5:150069856
Nucleotide Change
C>T
Most Severe Consequence
  • intron variant
See all consequences
HGVS.g name
  • (GRCh38)5:150069856C>T
HGVS.c name
  • ENSEMBL:ENST00000286301.7:c.1510+17G>A
  • ENSEMBL:ENST00000504875.5:n.1673+17G>A
HGVS.p name
Not Available
Synonyms
Not Available
Notes
Not Available
Cross references
Not Available
References
Not Available
Genome location
Assembly version
Not Available
Viewer Help
Data currently unavailable; sequence viewer under construction

Variant Molecular Consequences

Sequence feature
Sequence feature type
Associated gene
Location
Molecular consequence
Codon and amino acid change
ENSEMBL:ENST00000286301.7
protein_codingCSF1RIntron 10/21
  • intron variant
ENSEMBL:ENST00000504875.5
transcriptCSF1RIntron 9/19
  • intron variant
ENSEMBL:ENST00000675795.1
protein_codingCSF1RIntron 9/20
  • intron variant
RefSeq:NM_001288705.3
protein_codingCSF1RIntron 9/20
  • intron variant
RefSeq:NM_001349736.2
protein_codingCSF1RIntron 11/22
  • intron variant
RefSeq:NM_005211.4
protein_codingCSF1RIntron 11/22
  • intron variant
RefSeq:NR_109969.2
transcriptCSF1RIntron 9/19
  • intron variant
RefSeq:NR_164679.1
transcriptCSF1RIntron 9/19
  • intron variant
Showing 1 - 8 of 8 rows
per page