List of variants in gene FAT4 reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_001291303.3(FAT4):c.7199+91C>T	rs80234380	0.02324
NM_001291303.3(FAT4):c.10810A>C (p.Ile3604Leu)	rs76491994	0.01009
NM_001291303.3(FAT4):c.12299+52T>C	rs115877455	0.00727
NM_001291303.3(FAT4):c.4154T>C (p.Leu1385Ser)	rs139883132	0.00597
NM_001291303.3(FAT4):c.12986A>G (p.Asp4329Gly)	rs114234553	0.00519
NM_001291303.3(FAT4):c.14663C>G (p.Ala4888Gly)	rs35340865	0.00515
NM_001291303.3(FAT4):c.5921-23T>A	rs374890941	0.00458
NM_001291303.3(FAT4):c.6733G>A (p.Val2245Ile)	rs112971995	0.00426
NM_001291303.3(FAT4):c.10853C>T (p.Thr3618Met)	rs111423173	0.00407
NM_001291303.3(FAT4):c.12855T>C (p.Asp4285=)	rs78040862	0.00362
NM_001291303.3(FAT4):c.7358G>T (p.Ser2453Ile)	rs72914988	0.00327
NM_001291303.3(FAT4):c.13554G>A (p.Leu4518=)	rs78235204	0.00273
NM_001291303.3(FAT4):c.7935C>T (p.Asp2645=)	rs146157250	0.00244
NM_001291303.3(FAT4):c.524G>T (p.Arg175Leu)	rs143534324	0.00217
NM_001291303.3(FAT4):c.14159C>G (p.Ala4720Gly)	rs76607227	0.00206
NM_001291303.3(FAT4):c.1855C>T (p.Arg619Cys)	rs202125547	0.00121
NM_001291303.3(FAT4):c.14940A>G (p.Glu4980=)	rs149073729	0.00088
NM_001291303.3(FAT4):c.11670C>T (p.Cys3890=)	rs150894545	0.00086
NM_001291303.3(FAT4):c.11619C>T (p.Cys3873=)	rs141328606	0.00084
NM_001291303.3(FAT4):c.3962T>C (p.Phe1321Ser)	rs147900577	0.00070
NM_001291303.3(FAT4):c.9810G>A (p.Val3270=)	rs139518045	0.00062
NM_001291303.3(FAT4):c.10392C>A (p.Ile3464=)	rs140494092	0.00029
NM_001291303.3(FAT4):c.9141C>T (p.Ser3047=)	rs146492311	0.00024
NM_001291303.3(FAT4):c.761A>T (p.His254Leu)	rs201036193	0.00019
NM_001291303.3(FAT4):c.14325G>A (p.Pro4775=)	rs758537642	0.00013
NM_001291303.3(FAT4):c.13828G>A (p.Ala4610Thr)	rs142894845	0.00006
NM_001291303.3(FAT4):c.4599C>T (p.Asn1533=)	rs371858685	0.00005
NM_001291303.3(FAT4):c.14430A>G (p.Ala4810=)	rs144297905	0.00003
NM_001291303.3(FAT4):c.13416C>T (p.Gly4472=)	rs141983394	0.00002
NM_001291303.3(FAT4):c.7966A>C (p.Lys2656Gln)	rs760398912	0.00002
NM_001291303.3(FAT4):c.13260G>A (p.Gln4420=)	rs770683738	0.00001
NM_001291303.3(FAT4):c.3315C>T (p.Tyr1105=)	rs374329069	0.00001
NM_001291303.3(FAT4):c.2316A>G (p.Gln772=)	rs187427286

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