"PreventionGenetics, part of Exact Sciences"[submitter] AND "IL31RA"[g - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044376	NM_139017.7(IL31RA):c.33G>C (p.Thr11=)	IL31RA	Single nucleotide variant (synonymous variant +1 more)	IL31RA-related disorder	GLikely benign
Select item 3056087	NM_139017.7(IL31RA):c.307A>G (p.Asn103Asp)	IL31RA (N103D +1 more)	Single nucleotide variant (missense variant +1 more)	IL31RA-related disorder	GBenign
Select item 3053875	NM_139017.7(IL31RA):c.606+10G>T	IL31RA	Single nucleotide variant (intron variant)	IL31RA-related disorder	GLikely benign
Select item 735802	NM_139017.7(IL31RA):c.709G>A (p.Val237Ile)	IL31RA (V237I +2 more)	Single nucleotide variant (missense variant)	IL31RA-related disorder +2 more	GConflicting classifications of pathogenicity
Select item 785124	NM_139017.7(IL31RA):c.773-9T>C	IL31RA	Single nucleotide variant (intron variant)	IL31RA-related disorder +1 more	GBenign
Select item 3046483	NM_139017.7(IL31RA):c.804G>A (p.Leu268=)	IL31RA	Single nucleotide variant (synonymous variant)	IL31RA-related disorder	GLikely benign
Select item 1098854	NM_139017.7(IL31RA):c.1449T>G (p.Gly483=)	IL31RA	Single nucleotide variant (synonymous variant)	IL31RA-related disorder +1 more	GBenign
Select item 3035433	NM_139017.7(IL31RA):c.1501+79C>T	IL31RA (A527V)	Single nucleotide variant (missense variant +1 more)	IL31RA-related disorder	GBenign
Select item 3060128	NM_139017.7(IL31RA):c.1586G>A (p.Ser529Asn)	IL31RA (S387N +2 more)	Single nucleotide variant (missense variant)	IL31RA-related disorder	GBenign
Select item 3037234	NM_139017.7(IL31RA):c.1764C>T (p.Thr588=)	IL31RA	Single nucleotide variant (synonymous variant)	IL31RA-related disorder	GBenign
Select item 3056541	NM_139017.7(IL31RA):c.2014G>C (p.Val672Leu)	IL31RA (V530L +2 more)	Single nucleotide variant (missense variant +1 more)	IL31RA-related disorder	GBenign