ClinVar Miner

List of variants studied for demyelinating disease by Demyelinating Disease Laboratories, VA Medical Center and University of Tennessee

Included ClinVar conditions (16):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_031157.4(HNRNPA1):c.911G>A (p.Ser304Asn) rs483353020 0.00003
NM_031157.4(HNRNPA1):c.949A>G (p.Asn317Asp) rs483353023 0.00001
NM_031157.4(HNRNPA1):c.1006A>G (p.Arg336Gly) rs483353032
NM_031157.4(HNRNPA1):c.1009A>G (p.Ser337Gly) rs483353033
NM_031157.4(HNRNPA1):c.1040A>G (p.Tyr347Cys) rs483353034
NM_031157.4(HNRNPA1):c.1042T>C (p.Phe348Leu) rs483353035
NM_031157.4(HNRNPA1):c.1052C>T (p.Pro351Leu) rs483353036
NM_031157.4(HNRNPA1):c.1054C>T (p.Arg352Ter) rs483353037
NM_031157.4(HNRNPA1):c.1057A>G (p.Asn353Asp) rs483353039
NM_031157.4(HNRNPA1):c.1058A>G (p.Asn353Ser) rs483353038
NM_031157.4(HNRNPA1):c.1078T>G (p.Ser360Ala) rs483353040
NM_031157.4(HNRNPA1):c.1093A>G (p.Ser365Gly) rs483353026
NM_031157.4(HNRNPA1):c.1096T>C (p.Tyr366His) rs483353027
NM_031157.4(HNRNPA1):c.1097A>G (p.Tyr366Cys) rs483353041
NM_031157.4(HNRNPA1):c.1106G>A (p.Gly369Asp) rs483353042
NM_031157.4(HNRNPA1):c.1111A>G (p.Arg371Gly) rs3206707
NM_031157.4(HNRNPA1):c.1114T>C (p.Phe372Leu) rs483353043
NM_031157.4(HNRNPA1):c.931A>G (p.Ser311Gly) rs483353021
NM_031157.4(HNRNPA1):c.943T>C (p.Phe315Leu) rs483353022
NM_031157.4(HNRNPA1):c.973T>C (p.Phe325Leu) rs483353028
NM_031157.4(HNRNPA1):c.973T>G (p.Phe325Val) rs483353028
NM_031157.4(HNRNPA1):c.979C>T (p.Pro327Ser) rs483353029
NM_031157.4(HNRNPA1):c.982A>C (p.Met328Leu) rs483353024
NM_031157.4(HNRNPA1):c.987G>T (p.Lys329Asn) rs483353030
NM_031157.4(HNRNPA1):c.995A>G (p.Asn332Ser) rs3207617
NM_031157.4(HNRNPA1):c.997T>C (p.Phe333Leu) rs483353031

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