List of variants in gene TGIF1 reported as likely benign for developmental defect during embryogenesis

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

Total variants: 28

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HGVS	dbSNP	gnomAD frequency
NM_003244.4(TGIF1):c.420A>G (p.Pro140=)	rs2229337	0.13985
NM_003244.4(TGIF1):c.487C>T (p.Pro163Ser)	rs4468717	0.06068
NM_003244.4(TGIF1):c.657T>G (p.Thr219=)	rs2229336	0.05610
NM_003244.4(TGIF1):c.488C>T (p.Pro163Leu)	rs2229333	0.04416
NM_003244.4(TGIF1):c.576C>T (p.Val192=)	rs2229335	0.04112
NM_003244.4(TGIF1):c.*407C>G	rs115682894	0.01162
NM_003244.4(TGIF1):c.320A>T (p.Gln107Leu)	rs28939693	0.00048
NM_003244.4(TGIF1):c.*19A>G	rs145621092	0.00039
NM_003244.4(TGIF1):c.723G>A (p.Pro241=)	rs114912664	0.00039
NM_003244.4(TGIF1):c.573G>T (p.Ser191=)	rs142737563	0.00016
NM_003244.4(TGIF1):c.225A>G (p.Thr75=)	rs142830828	0.00014
NM_003244.4(TGIF1):c.711C>A (p.Pro237=)	rs141303152	0.00011
NM_003244.4(TGIF1):c.16+10C>T	rs373881756	0.00004
NM_003244.4(TGIF1):c.451A>G (p.Thr151Ala)	rs121909068	0.00004
NM_003244.4(TGIF1):c.90C>T (p.Ser30=)	rs760906198	0.00004
NM_003244.4(TGIF1):c.612G>C (p.Ala204=)	rs775764296	0.00003
NM_003244.4(TGIF1):c.264C>T (p.Asn88=)	rs375583740	0.00002
NM_003244.4(TGIF1):c.16+11C>G	rs879781590	0.00001
NM_003244.4(TGIF1):c.16+14G>A	rs746063172	0.00001
NM_003244.4(TGIF1):c.408A>G (p.Leu136=)	rs772528947	0.00001
NM_003244.4(TGIF1):c.810T>C (p.Leu270=)	rs766739006	0.00001
NM_003244.4(TGIF1):c.*441del	rs397858239
NM_003244.4(TGIF1):c.124C>T (p.Leu42=)
NM_003244.4(TGIF1):c.16+9G>A
NM_003244.4(TGIF1):c.244-13G>A
NM_003244.4(TGIF1):c.244-19C>T
NM_003244.4(TGIF1):c.288C>T (p.Asp96=)	rs2143416759
NM_003244.4(TGIF1):c.678G>A (p.Thr226=)

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