List of variants in gene STAT5B reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_012448.4(STAT5B):c.247C>T (p.Leu83=)	rs146176992	0.00415
NM_012448.4(STAT5B):c.551-5T>C	rs200299299	0.00188
NM_012448.4(STAT5B):c.795C>T (p.Gly265=)	rs766796346	0.00037
NM_012448.4(STAT5B):c.1569G>A (p.Arg523=)	rs143172354	0.00034
NM_012448.4(STAT5B):c.13A>T (p.Ile5Leu)	rs376041480	0.00014
NM_012448.4(STAT5B):c.944A>C (p.Glu315Ala)	rs572536541	0.00012
NM_012448.4(STAT5B):c.59C>T (p.Ala20Val)	rs935891734	0.00002
NM_012448.4(STAT5B):c.2259C>T (p.Thr753=)	rs776893445	0.00001
GRCh37/hg19 17q21.2(chr17:40371730-40371860)x1
NM_012448.4(STAT5B):c.1454A>G (p.Asp485Gly)
NM_012448.4(STAT5B):c.1474-2_1474delinsT
NM_012448.4(STAT5B):c.173C>T (p.Thr58Ile)
NM_012448.4(STAT5B):c.1924A>C (p.Asn642His)	rs938448224
NM_012448.4(STAT5B):c.2135_2139dup (p.Ala714Ter)
NM_012448.4(STAT5B):c.2186C>T (p.Ala729Val)	rs1598292092
NM_012448.4(STAT5B):c.322T>A (p.Cys108Ser)	rs2080259763

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