List of variants in gene SALL1 reported as likely benign for Townes-Brocks syndrome 1

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 33

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HGVS	dbSNP
NM_001127892.1(SALL1):c.83_87GCCCC[1]	rs374006676
NM_001127892.1(SALL1):c.157_159AGC[7] (p.Ser60_Ser62del)	rs113614842
NM_002968.2(SALL1):c.*1112dup	rs551203456
NM_002968.2(SALL1):c.*192T>C	rs3743767
NM_002968.2(SALL1):c.*437C>A	rs371127619
NM_002968.2(SALL1):c.*550G>T	rs377665001
NM_002968.2(SALL1):c.*646C>T	rs143159240
NM_002968.2(SALL1):c.*922T>G	rs184690178
NM_002968.2(SALL1):c.1006G>A (p.Gly336Ser)	rs776766459
NM_002968.2(SALL1):c.129C>T (p.His43=)	rs368688611
NM_002968.2(SALL1):c.1322C>A (p.Thr441Asn)	rs76275412
NM_002968.2(SALL1):c.1731C>G (p.Pro577=)	rs767216757
NM_002968.2(SALL1):c.1904C>T (p.Pro635Leu)	rs146454164
NM_002968.2(SALL1):c.2008T>C (p.Phe670Leu)	rs565545750
NM_002968.2(SALL1):c.2178G>A (p.Arg726=)	rs144019351
NM_002968.2(SALL1):c.220G>A (p.Val74Ile)	rs529479120
NM_002968.2(SALL1):c.2544A>G (p.Gln848=)	rs45459896
NM_002968.2(SALL1):c.263G>A (p.Ser88Asn)	rs760971365
NM_002968.2(SALL1):c.3120A>G (p.Thr1040=)	rs146655918
NM_002968.2(SALL1):c.3222G>A (p.Ala1074=)	rs61731131
NM_002968.2(SALL1):c.3711T>C (p.Tyr1237=)	rs3743768
NM_002968.2(SALL1):c.3794G>A (p.Gly1265Glu)	rs149302006
NM_002968.2(SALL1):c.379G>C (p.Val127Leu)	rs138635817
NM_002968.2(SALL1):c.3872A>G (p.Asn1291Ser)	rs74499562
NM_002968.2(SALL1):c.389C>T (p.Pro130Leu)	rs576713482
NM_002968.2(SALL1):c.390G>A (p.Pro130=)	rs75156807
NM_002968.2(SALL1):c.3915C>T (p.Asn1305=)	rs140524372
NM_002968.2(SALL1):c.3942C>T (p.Phe1314=)	rs189411650
NM_002968.2(SALL1):c.472A>G (p.Ser158Gly)	rs139646526
NM_002968.2(SALL1):c.478G>A (p.Gly160Ser)	rs199760974
NM_002968.2(SALL1):c.537C>T (p.Leu179=)	rs200539812
NM_002968.2(SALL1):c.676G>A (p.Val226Ile)	rs149603480
NM_002968.2(SALL1):c.76+10C>G	rs758439424

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