"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PCDHA12"[g - - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3024694	NM_018903.4(PCDHA12):c.299C>T (p.Ala100Val)	LOC112267934, PCDHA1 +12 more (A100V)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 3024695	NM_018903.4(PCDHA12):c.309T>C (p.Ser103=)	LOC112267934, PCDHA1 +12 more	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2655794	NM_018903.4(PCDHA12):c.768A>G (p.Gln256=)	PCDHA1, PCDHA10 +11 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655795	NM_018903.4(PCDHA12):c.1813G>T (p.Ala605Ser)	PCDHA6, PCDHA7 +11 more (A605S)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2655796	NM_018904.3(PCDHA13):c.292C>A (p.Arg98=)	PCDHA2, PCDHA1 +12 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655797	NM_018904.3(PCDHA13):c.1428G>C (p.Thr476=)	PCDHA1, PCDHA10 +12 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655798	NM_018902.5(PCDHA11):c.2391+12410G>A	PCDHA1, PCDHA10 +12 more (G546S)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2655799	NM_018907.4(PCDHA4):c.2385+74492C>A	PCDHA1, PCDHA10 +12 more (A599D)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2655800	NM_018904.3(PCDHA13):c.2164C>A (p.Arg722=)	PCDHA1, PCDHA10 +12 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655801	NM_018904.3(PCDHA13):c.2202G>A (p.Pro734=)	PCDHA1, PCDHA10 +12 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655802	NM_018898.5(PCDHAC1):c.1671T>C (p.Phe557=)	PCDHA9, PCDHA@ +13 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655803	NM_018899.6(PCDHAC2):c.480G>T (p.Ser160=)	PCDHA1, PCDHA10 +14 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655804	NM_018899.6(PCDHAC2):c.1161C>G (p.Leu387=)	PCDHA1, PCDHA10 +14 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2673031	NM_018899.6(PCDHAC2):c.1911G>A (p.Leu637=)	PCDHA1, PCDHA10 +14 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2655805	NM_018899.6(PCDHAC2):c.2460G>A (p.Ser820=)	PCDHA1, PCDHA10 +14 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 770914	NM_018903.4(PCDHA12):c.2492C>G (p.Pro831Arg)	PCDHA1, PCDHA10 +15 more (P576R +10 more)	Single nucleotide variant (missense variant)	PCDHA9-related condition +1 more	GBenign/Likely benign
Select item 425542	GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3	ARL10, ARL14EPL +511 more	Copy number gain	not provided	GLikely benign