Related gene-specific medical variations for Gene (Select 23392) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3087073	NM_001364929.1(ECPAS):c.-83+116G>T	ECPAS, LOC130002357	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3087070	NM_001364929.1(ECPAS):c.-83+105G>A	ECPAS, LOC130002357	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3087067	NM_001364929.1(ECPAS):c.-83+80C>G	ECPAS, LOC130002357	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3087059	NM_001364929.1(ECPAS):c.-83+42C>T	ECPAS, LOC130002357	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3087053	NM_001364929.1(ECPAS):c.-95G>A	ECPAS, LOC130002357 (G4S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087050	NM_001364929.1(ECPAS):c.-98A>T	ECPAS, LOC130002357 (T3S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087049	NM_001364929.1(ECPAS):c.-128G>C	ECPAS, LOC130002357	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3087046	NM_001364929.1(ECPAS):c.-138C>T	ECPAS, LOC130002357	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3087042	NM_001364929.1(ECPAS):c.-152C>T	ECPAS, LOC130002357	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3087035	NM_001364929.1(ECPAS):c.-200C>T	ECPAS, LOC130002357	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3087033	NM_001364929.1(ECPAS):c.-210G>C	ECPAS, LOC130002357	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 3087024	NM_001364929.1(ECPAS):c.-330G>C	ECPAS, LOC130002357	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2659428	NM_001364929.1(ECPAS):c.-83+130A>C	ECPAS, LOC130002357	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2535163	NM_001364929.1(ECPAS):c.-83+56G>A	ECPAS, LOC130002357	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2521689	NM_001364929.1(ECPAS):c.-83+60G>T	ECPAS, LOC130002357	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 2458433	NM_001364929.1(ECPAS):c.-150C>T	ECPAS, LOC130002357	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 1691120	NM_001364929.1(ECPAS):c.23-6768G>A	ECPAS	Single nucleotide variant (intron variant)	Vascular endothelial growth factor (VEGF) inhibitor response	Gassociation