"Ambry Genetics"[submitter] AND "PRR13"[gene] - ClinVar - NCBI

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

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File

Search results

Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2460746	NM_018457.4(PRR13):c.53T>C (p.Ile18Thr)	PRR13 (I18T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476428	NM_018457.4(PRR13):c.88C>T (p.Pro30Ser)	PRR13 (P30S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623403	NM_018457.4(PRR13):c.103C>T (p.Pro35Ser)	PRR13 (P35S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3219313	NM_018457.4(PRR13):c.311T>C (p.Ile104Thr)	PRR13 (I104T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594296	NM_018457.4(PRR13):c.392A>C (p.Lys131Thr)	PRR13 (K131T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

Display options Sort by Location Download

Format

Tabular
Tabular (text)
UI List

Sort by

Location
Relevance
Gene
Variation

Choose Destination

File