TTC39A[gene] and "single gene"[properties] - ClinVar

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

Search results

Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2343702	NM_001297663.2(TTC39A):c.1711A>G (p.Met571Val)	TTC39A (M148V +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292836	NM_001297663.2(TTC39A):c.1703G>A (p.Ser568Asn)	TTC39A (S569N +7 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3184346	NM_001297663.2(TTC39A):c.1592A>G (p.Lys531Arg)	TTC39A (K532R +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614020	NM_001297663.2(TTC39A):c.1570G>A (p.Asp524Asn)	TTC39A (D525N +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 487623	NM_001297663.2(TTC39A):c.1490C>G (p.Ala497Gly)	TTC39A (A501G +6 more)	Single nucleotide variant (missense variant)	Wolff-Parkinson-White pattern	GUncertain significance
Select item 2356252	NM_001297663.2(TTC39A):c.1479G>T (p.Arg493Ser)	TTC39A (R137S +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287949	NM_001297663.2(TTC39A):c.1401C>G (p.Asp467Glu)	TTC39A (D111E +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622945	NM_001297663.2(TTC39A):c.1360A>T (p.Met454Leu)	TTC39A (M427L +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517785	NM_001297663.2(TTC39A):c.1336G>C (p.Glu446Gln)	TTC39A (E446Q +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 487628	NM_001297663.2(TTC39A):c.1322C>T (p.Thr441Met)	TTC39A (T445M +6 more)	Single nucleotide variant (missense variant)	Wolff-Parkinson-White pattern	GUncertain significance
Select item 2286514	NM_001297663.2(TTC39A):c.1303G>A (p.Gly435Arg)	TTC39A (G408R +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3329894	NM_001297663.2(TTC39A):c.1297G>A (p.Val433Met)	TTC39A (V468M +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342670	NM_001297663.2(TTC39A):c.1173T>G (p.Ile391Met)	TTC39A (I364M +6 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370225	NM_001297663.2(TTC39A):c.1022A>T (p.Asp341Val)	TTC39A (D345V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391893	NM_001297663.2(TTC39A):c.1021G>A (p.Asp341Asn)	TTC39A (D376N +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405521	NM_001297663.2(TTC39A):c.928C>G (p.Gln310Glu)	TTC39A (Q311E +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381863	NM_001297663.2(TTC39A):c.901C>T (p.Arg301Cys)	TTC39A (R302C +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3329895	NM_001297663.2(TTC39A):c.821G>A (p.Arg274Gln)	TTC39A (R310Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590641	NM_001297663.2(TTC39A):c.820C>T (p.Arg274Trp)	TTC39A (R275W +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184347	NM_001297663.2(TTC39A):c.703C>T (p.Arg235Cys)	TTC39A (R271C +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638813	NM_001297663.2(TTC39A):c.645A>G (p.Ser215=)	TTC39A	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2480972	NM_001297663.2(TTC39A):c.500G>T (p.Ser167Ile)	TTC39A (S140I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405715	NM_001297663.2(TTC39A):c.241G>A (p.Gly81Ser)	TTC39A (G54S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612201	NM_001297663.2(TTC39A):c.46C>T (p.Pro16Ser)	TTC39A (P16S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 24