Related gene-specific medical variations for Gene (Select 4957) - 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 3250501	NM_001351578.2(ODF2):c.830+7T>C	ODF2, ODF2-AS1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3204048	NM_001351578.2(ODF2):c.691C>G (p.Arg231Gly)	ODF2, ODF2-AS1 (R124G +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2659536	NM_001351578.2(ODF2):c.2193G>A (p.Ala731=)	LOC113839524, ODF2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2620470	NM_001351578.2(ODF2):c.865T>C (p.Cys289Arg)	ODF2, ODF2-AS1 (C182R +10 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2405285	NM_001351578.2(ODF2):c.627G>T (p.Lys209Asn)	ODF2, ODF2-AS1 (K102N +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357306	NM_001351578.2(ODF2):c.803G>T (p.Arg268Leu)	ODF2, ODF2-AS1 (R104L +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342787	NM_001351578.2(ODF2):c.524C>T (p.Thr175Met)	ODF2, ODF2-AS1 (T117M +8 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2309613	NM_001351578.2(ODF2):c.799G>A (p.Glu267Lys)	ODF2, ODF2-AS1 (E103K +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292816	NM_001351578.2(ODF2):c.779C>T (p.Thr260Met)	ODF2, ODF2-AS1 (T153M +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290902	NM_001351578.2(ODF2):c.890C>T (p.Ala297Val)	ODF2, ODF2-AS1 (A133V +10 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2282087	NM_001351578.2(ODF2):c.647C>T (p.Ala216Val)	ODF2, ODF2-AS1 (A109V +8 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance