ClinVar Miner

List of variants in gene AFF2 reported by CeGaT Center for Human Genetics Tuebingen

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Total variants: 34
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HGVS dbSNP gnomAD frequency
NM_002025.4(AFF2):c.3088A>C (p.Ile1030Leu) rs149653283 0.00046
NM_002025.4(AFF2):c.2780G>A (p.Arg927His) rs140927355 0.00036
NM_002025.4(AFF2):c.1640G>A (p.Gly547Asp) rs147098255 0.00003
NM_002025.4(AFF2):c.2776C>T (p.Arg926Cys) rs1312069228 0.00002
NM_002025.4(AFF2):c.2913+7A>G rs1557288292 0.00001
NM_002025.4(AFF2):c.3138G>A (p.Ala1046=) rs974621684 0.00001
NM_002025.4(AFF2):c.1034C>A (p.Thr345Lys)
NM_002025.4(AFF2):c.1041+56413A>G
NM_002025.4(AFF2):c.1041+56438C>T
NM_002025.4(AFF2):c.1160C>A (p.Ser387Tyr)
NM_002025.4(AFF2):c.1330A>G (p.Thr444Ala)
NM_002025.4(AFF2):c.1467A>T (p.Glu489Asp) rs782268933
NM_002025.4(AFF2):c.1541G>A (p.Arg514His) rs369100046
NM_002025.4(AFF2):c.1625A>G (p.Lys542Arg) rs1603348128
NM_002025.4(AFF2):c.1692A>G (p.Gln564=)
NM_002025.4(AFF2):c.1861G>A (p.Val621Met)
NM_002025.4(AFF2):c.1871G>A (p.Arg624Lys)
NM_002025.4(AFF2):c.1992T>C (p.His664=)
NM_002025.4(AFF2):c.2009G>A (p.Arg670His) rs1569557647
NM_002025.4(AFF2):c.2082G>T (p.Lys694Asn) rs1603348350
NM_002025.4(AFF2):c.2171A>T (p.Gln724Leu)
NM_002025.4(AFF2):c.2205G>T (p.Pro735=) rs782504526
NM_002025.4(AFF2):c.234T>C (p.Tyr78=)
NM_002025.4(AFF2):c.2351T>G (p.Met784Arg)
NM_002025.4(AFF2):c.251T>C (p.Leu84Ser)
NM_002025.4(AFF2):c.2601G>A (p.Lys867=)
NM_002025.4(AFF2):c.2719A>G (p.Arg907Gly)
NM_002025.4(AFF2):c.2906C>T (p.Ser969Leu)
NM_002025.4(AFF2):c.2935G>C (p.Ala979Pro)
NM_002025.4(AFF2):c.3374C>T (p.Thr1125Ile)
NM_002025.4(AFF2):c.3872C>T (p.Thr1291Ile)
NM_002025.4(AFF2):c.407T>A (p.Met136Lys) rs782692812
NM_002025.4(AFF2):c.811C>T (p.Pro271Ser)
NM_002025.4(AFF2):c.864C>T (p.Tyr288=)

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