ClinVar Miner

List of variants in gene LAMA2 reported by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 76
Download table as spreadsheet
HGVS dbSNP
NM_000426.3(LAMA2):c.1262C>A (p.Ser421Tyr) rs775603569
NM_000426.3(LAMA2):c.1308T>G (p.Gly436=) rs41285286
NM_000426.3(LAMA2):c.1400A>G (p.Lys467Arg) rs138162760
NM_000426.3(LAMA2):c.1403C>G (p.Ala468Gly) rs111695726
NM_000426.3(LAMA2):c.1550A>T (p.Glu517Val) rs372358704
NM_000426.3(LAMA2):c.156C>T (p.Ile52=) rs1140366
NM_000426.3(LAMA2):c.1586G>A (p.Ser529Asn) rs370691060
NM_000426.3(LAMA2):c.1621A>G (p.Ser541Gly) rs141363186
NM_000426.3(LAMA2):c.1634T>A (p.Leu545Gln) rs118083923
NM_000426.3(LAMA2):c.1650C>T (p.Gly550=) rs899353
NM_000426.3(LAMA2):c.1681T>G (p.Leu561Val) rs765515681
NM_000426.3(LAMA2):c.1856G>A (p.Arg619His) rs3816665
NM_000426.3(LAMA2):c.1873A>G (p.Ile625Val) rs141658354
NM_000426.3(LAMA2):c.2121C>T (p.Ser707=)
NM_000426.3(LAMA2):c.2430A>C (p.Pro810=) rs147572139
NM_000426.3(LAMA2):c.2477G>A (p.Arg826Gln) rs759973830
NM_000426.3(LAMA2):c.2794A>G (p.Ser932Gly) rs761539740
NM_000426.3(LAMA2):c.2799A>G (p.Gln933=) rs1027199
NM_000426.3(LAMA2):c.3296A>G (p.Asn1099Ser) rs35065563
NM_000426.3(LAMA2):c.3317G>A (p.Cys1106Tyr) rs371548755
NM_000426.3(LAMA2):c.3532G>A (p.Ala1178Thr) rs34505698
NM_000426.3(LAMA2):c.3570T>C (p.Ala1190=) rs373757863
NM_000426.3(LAMA2):c.381C>A (p.Thr127=) rs4404787
NM_000426.3(LAMA2):c.3924+2T>C rs1554269966
NM_000426.3(LAMA2):c.411G>A (p.Ala137=) rs149347601
NM_000426.3(LAMA2):c.4321C>A (p.His1441Asn) rs1562477412
NM_000426.3(LAMA2):c.4437-5T>A rs41285288
NM_000426.3(LAMA2):c.4487C>T (p.Ala1496Val) rs147077184
NM_000426.3(LAMA2):c.479A>T (p.Asp160Val) rs147398243
NM_000426.3(LAMA2):c.488A>T (p.Tyr163Phe) rs201175472
NM_000426.3(LAMA2):c.4909G>A (p.Glu1637Lys) rs138303386
NM_000426.3(LAMA2):c.4935C>A (p.Thr1645=) rs35579821
NM_000426.3(LAMA2):c.4956C>G (p.Thr1652=) rs17057184
NM_000426.3(LAMA2):c.4969G>A (p.Val1657Met) rs370971334
NM_000426.3(LAMA2):c.5234+1G>A rs781376927
NM_000426.3(LAMA2):c.5247C>T (p.Ala1749=) rs149951387
NM_000426.3(LAMA2):c.5284C>G (p.Arg1762Gly) rs746492572
NM_000426.3(LAMA2):c.5291A>G (p.Glu1764Gly) rs141950826
NM_000426.3(LAMA2):c.5466A>G (p.Glu1822=) rs3749877
NM_000426.3(LAMA2):c.5689G>A (p.Ala1897Thr) rs200518204
NM_000426.3(LAMA2):c.5909G>C (p.Cys1970Ser) rs148451013
NM_000426.3(LAMA2):c.6079C>A (p.Pro2027Thr) rs374006928
NM_000426.3(LAMA2):c.6150T>C (p.Asp2050=) rs114766691
NM_000426.3(LAMA2):c.6158C>T (p.Ala2053Val) rs1562566133
NM_000426.3(LAMA2):c.6161A>G (p.Gln2054Arg) rs56035053
NM_000426.3(LAMA2):c.6274+4C>T rs73775410
NM_000426.3(LAMA2):c.6429+8C>A rs199773264
NM_000426.3(LAMA2):c.6518A>T (p.Asn2173Ile) rs529110314
NM_000426.3(LAMA2):c.6539A>T (p.Asp2180Val) rs567385461
NM_000426.3(LAMA2):c.6659C>T (p.Pro2220Leu) rs367665458
NM_000426.3(LAMA2):c.675C>T (p.Ala225=) rs139665175
NM_000426.3(LAMA2):c.6764T>C (p.Ile2255Thr) rs951339046
NM_000426.3(LAMA2):c.6952T>A (p.Phe2318Ile) rs757197871
NM_000426.3(LAMA2):c.7057C>T (p.Arg2353Cys) rs145885540
NM_000426.3(LAMA2):c.7074C>A (p.Tyr2358Ter) rs762806915
NM_000426.3(LAMA2):c.7118C>T (p.Ser2373Leu)
NM_000426.3(LAMA2):c.7346T>C (p.Ile2449Thr) rs1156828795
NM_000426.3(LAMA2):c.7395T>C (p.Asp2465=) rs140483001
NM_000426.3(LAMA2):c.7431A>T (p.Arg2477Ser) rs34367843
NM_000426.3(LAMA2):c.7760T>C (p.Val2587Ala) rs2229848
NM_000426.3(LAMA2):c.7830G>C (p.Val2610=) rs2229849
NM_000426.3(LAMA2):c.8011C>A (p.Pro2671Thr) rs780695627
NM_000426.3(LAMA2):c.8028T>C (p.Asn2676=) rs35313209
NM_000426.3(LAMA2):c.8147G>A (p.Arg2716His) rs142781107
NM_000426.3(LAMA2):c.8244+3_8244+6del rs746678525
NM_000426.3(LAMA2):c.8528A>G (p.Asn2843Ser) rs73599293
NM_000426.3(LAMA2):c.8548-10T>C rs113644365
NM_000426.3(LAMA2):c.8586T>C (p.Tyr2862=) rs142451929
NM_000426.3(LAMA2):c.8692A>C (p.Arg2898=) rs200718262
NM_000426.3(LAMA2):c.8755C>T (p.Pro2919Ser) rs143026295
NM_000426.3(LAMA2):c.9123C>T (p.Val3041=) rs61749497
NM_000426.3(LAMA2):c.922G>A (p.Glu308Lys) rs146462599
NM_001079823.2(LAMA2):c.2325C>A (p.Asn775Lys)
NM_001079823.2(LAMA2):c.4909G>C (p.Glu1637Gln)
NM_001079823.2(LAMA2):c.5899G>T (p.Ala1967Ser)
NM_001079823.2(LAMA2):c.9089_9092dup (p.His3031fs) rs398123390

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.