List of variants in gene FTCD reported as pathogenic for hematologic disorder

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_206965.2(FTCD):c.1607T>A (p.Leu536Ter)	rs149266909	0.00116
NM_206965.2(FTCD):c.211C>T (p.Arg71Ter)	rs8133955	0.00021
NM_206965.2(FTCD):c.403C>T (p.Arg135Cys)	rs28941768	0.00006
NM_206965.2(FTCD):c.763C>T (p.Arg255Ter)	rs140217223	0.00003
NC_000021.8:g.(?_47565311)_(47575437_?)del
NM_206965.2(FTCD):c.1366dup (p.Glu456fs)	rs777099958
NM_206965.2(FTCD):c.293dup (p.Val99fs)	rs1310075515
NM_206965.2(FTCD):c.372C>G (p.Tyr124Ter)
NM_206965.2(FTCD):c.378C>G (p.Tyr126Ter)	rs374724805
NM_206965.2(FTCD):c.896G>C (p.Arg299Pro)	rs119469015
NM_206965.2(FTCD):c.990dup (p.Pro331fs)	rs398124234

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