Related gene-specific medical variations for Gene (Select 5733) - ClinVar - NCBI

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

Links from Gene

Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3220727	NM_198719.2(PTGER3):c.820G>A (p.Gly274Ser)	PTGER3, ZRANB2-AS1 (G274S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3220726	NM_198719.2(PTGER3):c.694T>C (p.Ser232Pro)	PTGER3, ZRANB2-AS1 (S232P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3220725	NM_198719.2(PTGER3):c.490T>C (p.Trp164Arg)	PTGER3, ZRANB2-AS1 (W164R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3220724	NM_198719.2(PTGER3):c.47G>A (p.Arg16His)	PTGER3, ZRANB2-AS1 (R16H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3220723	NM_198719.2(PTGER3):c.214C>T (p.Leu72Phe)	PTGER3, ZRANB2-AS1 (L72F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2559833	NM_198719.2(PTGER3):c.121C>G (p.Pro41Ala)	PTGER3, ZRANB2-AS1 (P41A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2297485	NM_198719.2(PTGER3):c.64A>C (p.Thr22Pro)	PTGER3, ZRANB2-AS1 (T22P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2224214	NM_198719.2(PTGER3):c.23G>A (p.Gly8Glu)	PTGER3, ZRANB2-AS1 (G8E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 814094	GRCh37/hg19 1p31.1(chr1:71366112-71468493)x1	PTGER3	Copy number loss	not provided	GUncertain significance
Select item 777911	NM_198719.2(PTGER3):c.111C>G (p.Leu37=)	PTGER3, ZRANB2-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 152784	GRCh38/hg38 1p31.1(chr1:70907033-70991687)x1	PTGER3	Copy number loss	See cases	GUncertain significance