List of variants in gene EPHB4 reported as benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 35

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HGVS	dbSNP	gnomAD frequency
NM_004444.5(EPHB4):c.1297+168G>T	rs314367	0.97746
NM_004444.5(EPHB4):c.1871-41T>C	rs314358	0.57183
NM_004444.5(EPHB4):c.1752A>G (p.Gly584=)	rs314359	0.56302
NM_004444.5(EPHB4):c.1890C>T (p.Cys630=)	rs2230585	0.32230
NM_004444.5(EPHB4):c.2835-221T>C	rs221005	0.25636
NM_004444.5(EPHB4):c.546T>C (p.Gly182=)	rs56173078	0.09185
NM_004444.5(EPHB4):c.411+165C>T	rs73172605	0.09144
NM_004444.5(EPHB4):c.124-112G>A	rs41280998	0.09139
NM_004444.5(EPHB4):c.123+44G>A	rs41280995	0.09106
NM_004444.5(EPHB4):c.1422+90T>C	rs73170800	0.09026
NM_004444.5(EPHB4):c.1422+3A>G	rs3857809	0.08906
NM_004444.5(EPHB4):c.1588+66A>C	rs117772736	0.05706
NM_004444.5(EPHB4):c.2835-237C>T	rs2437101	0.04607
NM_004444.5(EPHB4):c.489G>A (p.Thr163=)	rs61130921	0.02793
NM_004444.5(EPHB4):c.1423-173A>T	rs74491853	0.02048
NM_004444.5(EPHB4):c.1692-34A>G	rs74340862	0.01976
NM_004444.5(EPHB4):c.2835-196C>G	rs78069730	0.01974
NM_004444.5(EPHB4):c.1588+27G>A	rs116672851	0.01959
NM_004444.5(EPHB4):c.1589-45A>G	rs28444497	0.00530
NM_004444.5(EPHB4):c.*134GA[2]	rs113576131
NM_004444.5(EPHB4):c.1298-66A>T	rs314364
NM_004444.5(EPHB4):c.1298-88C>G	rs314365
NM_004444.5(EPHB4):c.1314T>C (p.Ser438=)	rs144173
NM_004444.5(EPHB4):c.1588+104_1588+109del	rs35304729
NM_004444.5(EPHB4):c.1588+107_1588+109del	rs35304729
NM_004444.5(EPHB4):c.1588+108_1588+109del	rs35304729
NM_004444.5(EPHB4):c.1588+88_1588+89dup	rs35304729
NM_004444.5(EPHB4):c.1588+88dup	rs35304729
NM_004444.5(EPHB4):c.1589-232C>T	rs3890144
NM_004444.5(EPHB4):c.1757-121_1757-120dup	rs750195537
NM_004444.5(EPHB4):c.1757-121dup	rs750195537
NM_004444.5(EPHB4):c.2835-58A>C	rs314348
NM_004444.5(EPHB4):c.2949G>T (p.Pro983=)	rs112803997
NM_004444.5(EPHB4):c.809-186_809-185dup	rs11447690
NM_004444.5(EPHB4):c.809-186dup	rs11447690

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