All transcript variants in gene CSF1R

Information The variants shown are described using the NM_005211.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. - c.1237G>A likely benign r.(?) p.(Gly413Ser) g.149449827C>T - CSF1R(NM_005211.3):c.1237G>A (p.G413S) - CSF1R_000019 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_VUmc
?/. - c.1237G>A VUS r.(?) p.(Gly413Ser) g.149449827C>T - CSF1R(NM_005211.3):c.1237G>A (p.G413S) - CSF1R_000019 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Leiden
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