"PreventionGenetics, part of Exact Sciences"[submitter] AND "IL17RD"[g - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 50869	NM_017563.5(IL17RD):c.2204C>T (p.Ala735Val)	IL17RD (A735V +1 more)	Single nucleotide variant (missense variant)	IL17RD-related condition	GUncertain significance
Select item 3054167	NM_017563.5(IL17RD):c.1986A>G (p.Ser662=)	IL17RD, LOC126806689	Single nucleotide variant (synonymous variant)	IL17RD-related condition	GLikely benign
Select item 677804	NM_017563.5(IL17RD):c.1972A>G (p.Met658Val)	IL17RD, LOC126806689 (M658V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3043465	NM_017563.5(IL17RD):c.1968G>T (p.Ser656=)	IL17RD, LOC126806689	Single nucleotide variant (synonymous variant)	IL17RD-related condition	GLikely benign
Select item 787793	NM_017563.5(IL17RD):c.1697C>T (p.Pro566Leu)	IL17RD, LOC126806689 (P422L +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 731215	NM_017563.5(IL17RD):c.1656T>C (p.Phe552=)	IL17RD, LOC126806689	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3042330	NM_017563.5(IL17RD):c.1548C>T (p.His516=)	IL17RD, LOC126806689	Single nucleotide variant (synonymous variant)	IL17RD-related condition	GLikely benign
Select item 712436	NM_017563.5(IL17RD):c.1545C>T (p.Asp515=)	IL17RD, LOC126806689	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 723666	NM_017563.5(IL17RD):c.1383C>T (p.Leu461=)	IL17RD, LOC126806689	Single nucleotide variant (synonymous variant)	IL17RD-related condition +1 more	GBenign
Select item 721816	NM_017563.5(IL17RD):c.948C>A (p.Leu316=)	IL17RD	Single nucleotide variant (synonymous variant)	IL17RD-related condition +1 more	GLikely benign
Select item 731960	NM_017563.5(IL17RD):c.893T>C (p.Ile298Thr)	IL17RD (I298T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 731021	NM_017563.5(IL17RD):c.858C>T (p.Ala286=)	IL17RD	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3041790	NM_017563.5(IL17RD):c.558C>T (p.Asp186=)	IL17RD	Single nucleotide variant (synonymous variant)	IL17RD-related condition	GLikely benign
Select item 3053638	NM_017563.5(IL17RD):c.548G>A (p.Arg183Gln)	IL17RD (R183Q +1 more)	Single nucleotide variant (missense variant)	IL17RD-related condition	GUncertain significance
Select item 2063168	NM_017563.5(IL17RD):c.226G>A (p.Ala76Thr)	IL17RD (A76T)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 3058117	NM_017563.5(IL17RD):c.159G>A (p.Leu53=)	IL17RD	Single nucleotide variant (synonymous variant +1 more)	IL17RD-related condition	GLikely benign