List of variants in gene GRIN2A 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: 101

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HGVS	dbSNP	gnomAD frequency
NM_001134407.3(GRIN2A):c.2966A>G (p.Asn989Ser)	rs531782747	0.00005
NM_001134407.3(GRIN2A):c.1343A>G (p.Glu448Gly)	rs1273711716	0.00001
NM_001134407.3(GRIN2A):c.1783_1784del (p.His595fs)	rs779219028	0.00001
NM_000833.3:c.(?_-310-1)_(414+1_415-1)del
NM_001134407.3(GRIN2A):c.1001T>A (p.Leu334Ter)	rs1555455521
NM_001134407.3(GRIN2A):c.1007+1G>A	rs397518465
NM_001134407.3(GRIN2A):c.1036A>T (p.Lys346Ter)	rs2141482042
NM_001134407.3(GRIN2A):c.1123-1G>T	rs2042854251
NM_001134407.3(GRIN2A):c.1123-2A>G	rs397518469
NM_001134407.3(GRIN2A):c.1232T>A (p.Leu411Gln)	rs2141369514
NM_001134407.3(GRIN2A):c.1306T>C (p.Cys436Arg)	rs1555496111
NM_001134407.3(GRIN2A):c.1344_1345insCCTAG (p.Gly449fs)	rs2141346061
NM_001134407.3(GRIN2A):c.1362del (p.Lys454fs)
NM_001134407.3(GRIN2A):c.1400T>A (p.Leu467His)	rs2042668320
NM_001134407.3(GRIN2A):c.1447G>A (p.Gly483Arg)	rs2042667149
NM_001134407.3(GRIN2A):c.1492G>A (p.Gly498Ser)	rs757713617
NM_001134407.3(GRIN2A):c.1497+1G>C	rs2141344569
NM_001134407.3(GRIN2A):c.1552C>T (p.Arg518Cys)	rs747838255
NM_001134407.3(GRIN2A):c.1553G>A (p.Arg518His)	rs397518470
NM_001134407.3(GRIN2A):c.1579C>A (p.Pro527Thr)
NM_001134407.3(GRIN2A):c.1585del (p.Val529fs)	rs2141342590
NM_001134407.3(GRIN2A):c.1586del (p.Val529fs)	rs2141342580
NM_001134407.3(GRIN2A):c.1592C>T (p.Thr531Met)	rs397518468
NM_001134407.3(GRIN2A):c.1595G>T (p.Gly532Val)	rs1085307961
NM_001134407.3(GRIN2A):c.1613C>G (p.Ser538Ter)	rs2141342254
NM_001134407.3(GRIN2A):c.1642G>A (p.Ala548Thr)	rs1057523843
NM_001134407.3(GRIN2A):c.1642G>C (p.Ala548Pro)	rs1057523843
NM_001134407.3(GRIN2A):c.1651+1del	rs2141341804
NM_001134407.3(GRIN2A):c.1655C>G (p.Pro552Arg)	rs397518450
NM_001134407.3(GRIN2A):c.165G>A (p.Trp55Ter)	rs1057521810
NM_001134407.3(GRIN2A):c.1686del (p.Phe562fs)	rs2141325598
NM_001134407.3(GRIN2A):c.1692del (p.Met564fs)	rs886039604
NM_001134407.3(GRIN2A):c.172G>T (p.Glu58Ter)	rs143833346
NM_001134407.3(GRIN2A):c.176_179dup (p.Ala61fs)	rs2050235998
NM_001134407.3(GRIN2A):c.1782_1783insTT (p.His595fs)	rs2141313067
NM_001134407.3(GRIN2A):c.1818G>A (p.Trp606Ter)	rs775819322
NM_001134407.3(GRIN2A):c.1832T>A (p.Leu611Gln)	rs2141312803
NM_001134407.3(GRIN2A):c.1841A>G (p.Asn614Ser)	rs869312916
NM_001134407.3(GRIN2A):c.1845C>A (p.Asn615Lys)	rs397518447
NM_001134407.3(GRIN2A):c.1903G>A (p.Ala635Thr)	rs2042449005
NM_001134407.3(GRIN2A):c.1930A>G (p.Ser644Gly)	rs1555492763
NM_001134407.3(GRIN2A):c.1936A>G (p.Thr646Ala)	rs1555492758
NM_001134407.3(GRIN2A):c.1943A>G (p.Asn648Ser)	rs796052545
NM_001134407.3(GRIN2A):c.1945C>G (p.Leu649Val)	rs397514557
NM_001134407.3(GRIN2A):c.1946_1947delinsCT (p.Leu649Pro)
NM_001134407.3(GRIN2A):c.1954T>G (p.Phe652Val)	rs397518471
NM_001134407.3(GRIN2A):c.1957A>G (p.Met653Val)	rs2141312286
NM_001134407.3(GRIN2A):c.1959G>A (p.Met653Ile)	rs2141312277
NM_001134407.3(GRIN2A):c.1961T>C (p.Ile654Thr)	rs2042447540
NM_001134407.3(GRIN2A):c.2007+1G>A	rs2141312109
NM_001134407.3(GRIN2A):c.2007+2dup	rs2141312103
NM_001134407.3(GRIN2A):c.2008-1G>T	rs2141295189
NM_001134407.3(GRIN2A):c.2041C>T (p.Arg681Ter)	rs397518472
NM_001134407.3(GRIN2A):c.2042G>A (p.Arg681Gln)	rs753203288
NM_001134407.3(GRIN2A):c.2047G>C (p.Gly683Arg)
NM_001134407.3(GRIN2A):c.2050A>G (p.Thr684Ala)	rs796052547
NM_001134407.3(GRIN2A):c.2063G>C (p.Gly688Ala)	rs2141294973
NM_001134407.3(GRIN2A):c.2077A>G (p.Asn693Asp)	rs2042303226
NM_001134407.3(GRIN2A):c.2081T>C (p.Ile694Thr)	rs2141294911
NM_001134407.3(GRIN2A):c.2084G>A (p.Arg695Gln)	rs1555491654
NM_001134407.3(GRIN2A):c.2095C>T (p.Pro699Ser)	rs1555491648
NM_001134407.3(GRIN2A):c.2113A>G (p.Met705Val)	rs2141294795
NM_001134407.3(GRIN2A):c.2138T>G (p.Val713Gly)	rs1057518070
NM_001134407.3(GRIN2A):c.2140del (p.Glu714fs)	rs2141294703
NM_001134407.3(GRIN2A):c.2146G>A (p.Ala716Thr)
NM_001134407.3(GRIN2A):c.2191G>A (p.Asp731Asn)	rs796052549
NM_001134407.3(GRIN2A):c.2197G>A (p.Ala733Thr)	rs796052550
NM_001134407.3(GRIN2A):c.2221A>G (p.Arg741Gly)	rs1903135567
NM_001134407.3(GRIN2A):c.2253dup (p.Ser752fs)	rs2141230698
NM_001134407.3(GRIN2A):c.2278G>A (p.Gly760Ser)	rs1555488119
NM_001134407.3(GRIN2A):c.2326G>T (p.Asp776Tyr)	rs776791010
NM_001134407.3(GRIN2A):c.2334_2338del (p.Leu779fs)	rs2141230279
NM_001134407.3(GRIN2A):c.2335_2336delinsAG (p.Leu779Arg)	rs1903126465
NM_001134407.3(GRIN2A):c.2336T>G (p.Leu779Trp)	rs1555488084
NM_001134407.3(GRIN2A):c.2341_2343delinsAT (p.Gln781fs)	rs2141230262
NM_001134407.3(GRIN2A):c.236C>G (p.Pro79Arg)	rs1250662891
NM_001134407.3(GRIN2A):c.2384G>A (p.Trp795Ter)	rs1555483728
NM_001134407.3(GRIN2A):c.2407G>T (p.Glu803Ter)	rs1198247451
NM_001134407.3(GRIN2A):c.2408del (p.Glu803fs)	rs2141151209
NM_001134407.3(GRIN2A):c.2427C>A (p.Ser809Arg)	rs1064795647
NM_001134407.3(GRIN2A):c.2434C>A (p.Leu812Met)	rs752241086
NM_001134407.3(GRIN2A):c.2449A>G (p.Met817Val)	rs796052551
NM_001134407.3(GRIN2A):c.2450T>C (p.Met817Thr)	rs1064796608
NM_001134407.3(GRIN2A):c.2450T>G (p.Met817Arg)	rs1064796608
NM_001134407.3(GRIN2A):c.2453C>A (p.Ala818Glu)	rs751455326
NM_001134407.3(GRIN2A):c.2466C>G (p.Tyr822Ter)
NM_001134407.3(GRIN2A):c.254_261del (p.His85fs)
NM_001134407.3(GRIN2A):c.2844del (p.Gln950fs)
NM_001134407.3(GRIN2A):c.2T>C (p.Met1Thr)	rs397518466
NM_001134407.3(GRIN2A):c.3365G>A (p.Gly1122Asp)	rs760885908
NM_001134407.3(GRIN2A):c.415-2A>G	rs2141633312
NM_001134407.3(GRIN2A):c.487C>T (p.Gln163Ter)	rs1057524089
NM_001134407.3(GRIN2A):c.500G>A (p.Trp167Ter)	rs1555455776
NM_001134407.3(GRIN2A):c.551T>G (p.Ile184Ser)	rs2141632382
NM_001134407.3(GRIN2A):c.594G>A (p.Trp198Ter)	rs1555455726
NM_001134407.3(GRIN2A):c.627del (p.Phe210fs)	rs796052560
NM_001134407.3(GRIN2A):c.652C>T (p.Gln218Ter)	rs387906637
NM_001134407.3(GRIN2A):c.691T>C (p.Cys231Arg)	rs2141631426
NM_001134407.3(GRIN2A):c.692G>A (p.Cys231Tyr)	rs1238779318
NM_001134407.3(GRIN2A):c.730dup (p.Arg244fs)	rs2044762657
NM_001134407.3(GRIN2A):c.90dup (p.Pro31fs)	rs2142390867

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