"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "RNF151"[ge - ClinVar

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

Format

Sort by

Choose Destination

Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2645955	NM_174903.6(RNF151):c.149+8C>T	RNF151	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2645956	NM_174903.6(RNF151):c.201C>A (p.Val67=)	RNF151	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2498682	GRCh37/hg19 16p13.3(chr16:811896-2130379)x1	BAIAP3, C1QTNF8 +52 more	Copy number loss	not provided	GPathogenic

Format

Sort by

Choose Destination