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Variants
search result for
Homo sapiens
(View Results for all Objects and Ontologies)
5
records found for search term
Cfl1
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RGD ID
Symbol
Variant Type
Name
Trait
Clinical Significance
Chr
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Annotations
Match
150471730
CV1281056
single nucleotide variant
NM_005507.3(
CFL1
):c.198C>T (p.Asp66=)
not provided [RCV001713245]
benign
11
65856048
65856048
Human
name
155944273
CV2241969
single nucleotide variant
NM_005507.3(
CFL1
):c.203A>G (p.Tyr68Cys)
not specified [RCV004108920]
uncertain significance
11
65856043
65856043
Human
name
401767529
CV2727194
single nucleotide variant
NM_005507.3(
CFL1
):c.196G>A (p.Asp66Asn)
not specified [RCV004327332]
uncertain significance
11
65856050
65856050
Human
name
8634294
CV89514
single nucleotide variant
NM_005507.2(
CFL1
):c.296T>G (p.Leu99Arg)
Malignant melanoma [RCV000069611]
not provided
11
65855950
65855950
Human
name
407501933
CV3425429
single nucleotide variant
NM_005507.3(
CFL1
):c.436C>T (p.Arg146Cys)
not specified [RCV004607499]
uncertain significance
11
65855401
65855401
Human
name