List of variants in gene SALL1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 43

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HGVS	dbSNP	gnomAD frequency
NM_002968.3(SALL1):c.3872A>G (p.Asn1291Ser)	rs74499562	0.01024
NM_002968.3(SALL1):c.1903C>T (p.Pro635Ser)	rs61731136	0.00058
NM_002968.3(SALL1):c.129C>T (p.His43=)	rs368688611	0.00048
NM_002968.3(SALL1):c.1322C>A (p.Thr441Asn)	rs76275412	0.00034
NM_002968.3(SALL1):c.477C>A (p.Ser159Arg)	rs757737676	0.00028
NM_002968.3(SALL1):c.1327G>A (p.Asp443Asn)	rs374153597	0.00022
NM_002968.3(SALL1):c.1950C>T (p.Gly650=)	rs138705495	0.00019
NM_002968.3(SALL1):c.787G>T (p.Asp263Tyr)	rs567084895	0.00009
NM_002968.3(SALL1):c.3310C>G (p.Pro1104Ala)	rs547153228	0.00008
NM_002968.3(SALL1):c.1953C>T (p.Pro651=)	rs147169088	0.00007
NM_002968.3(SALL1):c.1992G>A (p.Pro664=)	rs754352358	0.00007
NM_002968.3(SALL1):c.2928C>T (p.His976=)	rs530363077	0.00006
NM_002968.3(SALL1):c.63C>T (p.Leu21=)	rs536125319	0.00006
NM_002968.3(SALL1):c.2121G>A (p.Glu707=)	rs759892297	0.00005
NM_002968.3(SALL1):c.24G>A (p.Lys8=)	rs759270242	0.00004
NM_002968.3(SALL1):c.2565T>G (p.Pro855=)	rs778734691	0.00004
NM_002968.3(SALL1):c.583G>A (p.Val195Ile)	rs546790476	0.00003
NM_002968.3(SALL1):c.3603C>T (p.Gly1201=)	rs542678985	0.00002
NM_002968.3(SALL1):c.*9G>A	rs753566942	0.00001
NM_002968.3(SALL1):c.1143C>T (p.Ser381=)	rs369940056	0.00001
NM_002968.3(SALL1):c.1527C>T (p.Asn509=)	rs1346104453	0.00001
NM_002968.3(SALL1):c.2008T>C (p.Phe670Leu)	rs565545750	0.00001
NM_002968.3(SALL1):c.220G>A (p.Val74Ile)	rs529479120	0.00001
NM_002968.3(SALL1):c.2397C>T (p.Pro799=)	rs752496655	0.00001
NM_002968.3(SALL1):c.2967C>T (p.Leu989=)	rs759617992	0.00001
NM_002968.3(SALL1):c.2055A>G (p.Ala685=)
NM_002968.3(SALL1):c.2643A>C (p.Leu881=)	rs1239088376
NM_002968.3(SALL1):c.270T>A (p.Pro90=)	rs2143452425
NM_002968.3(SALL1):c.2793G>A (p.Pro931=)	rs147312225
NM_002968.3(SALL1):c.2798_2803dup (p.Asn933_Ser934dup)	rs760807997
NM_002968.3(SALL1):c.3117C>T (p.Ser1039=)	rs2506483528
NM_002968.3(SALL1):c.3322G>A (p.Val1108Ile)	rs148931484
NM_002968.3(SALL1):c.3322G>C (p.Val1108Leu)	rs148931484
NM_002968.3(SALL1):c.3535-44CT[6]	rs142249003
NM_002968.3(SALL1):c.3855C>G (p.Leu1285=)	rs777335761
NM_002968.3(SALL1):c.472_475delinsG (p.Ser158_Ser159delinsGly)	rs2506497072
NM_002968.3(SALL1):c.478GGC[3] (p.Gly163del)	rs1555475414
NM_002968.3(SALL1):c.478GGC[5] (p.Gly163dup)	rs1555475414
NM_002968.3(SALL1):c.478GGC[6] (p.Gly163_Ser164insGlyGly)	rs1555475414
NM_002968.3(SALL1):c.639A>G (p.Glu213=)	rs1330085894
NM_002968.3(SALL1):c.76+26AC[5]	rs200502187
NM_002968.3(SALL1):c.801T>C (p.Ser267=)	rs745771993
NM_002968.3(SALL1):c.939G>T (p.Val313=)	rs1377611548

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