List of variants in gene ARID1B reported by Institute of Human Genetics, University of Leipzig Medical Center

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_001374828.1(ARID1B):c.2711G>A (p.Ser904Asn)	rs1159561275	0.00002
NM_001374828.1(ARID1B):c.1293_1320dup (p.Tyr441fs)
NM_001374828.1(ARID1B):c.1492del (p.Ala498fs)	rs1417035592
NM_001374828.1(ARID1B):c.1737del (p.Ser580fs)	rs1779022643
NM_001374828.1(ARID1B):c.1789C>T (p.Gln597Ter)	rs1779032666
NM_001374828.1(ARID1B):c.1987-29742G>A	rs1554261846
NM_001374828.1(ARID1B):c.2025C>G (p.Tyr675Ter)	rs773640553
NM_001374828.1(ARID1B):c.2287G>T (p.Glu763Ter)	rs1554294593
NM_001374828.1(ARID1B):c.2603_2606del (p.Arg868fs)	rs1085307695
NM_001374828.1(ARID1B):c.2762-3_2762-2delinsAG
NM_001374828.1(ARID1B):c.2956del (p.Ser985_Met986insTer)	rs2128634579
NM_001374828.1(ARID1B):c.3955dup (p.Gln1319fs)	rs1289067120
NM_001374828.1(ARID1B):c.5897G>T (p.Arg1966Leu)	rs758748419
NM_001374828.1(ARID1B):c.5916dup (p.Ser1974fs)	rs35441529
NM_001374828.1(ARID1B):c.6028del (p.Ala2010fs)	rs1794490994
NM_001374828.1(ARID1B):c.6751C>T (p.Arg2251Ter)	rs1554238072

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