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Items: 6

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr17:8390869
GRCh38:
Chr17:8487551
MYH10R1612Q, R1621Q, R1622Q, R1643Qnot providedUncertain significance
(Jan 1, 2021)
criteria provided, single submitterVCV001013379
2.
GRCh37:
Chr17:8393797
GRCh38:
Chr17:8490479
MYH10L1560P, L1551P, L1582P, L1561Pnot providedUncertain significance
(Oct 1, 2019)
criteria provided, single submitterVCV000872122
3.
GRCh37:
Chr17:8409701
GRCh38:
Chr17:8506383
MYH10not specifiedLikely benign
(Nov 13, 2018)
criteria provided, single submitterVCV000811078
4.
GRCh37:
Chr17:8390883
GRCh38:
Chr17:8487565
MYH10not providedLikely benign
(Apr 25, 2018)
criteria provided, single submitterVCV000618228
5.
GRCh37:
Chr17:8409746
GRCh38:
Chr17:8506428
MYH10D1092E, D1061E, D1070E, D1071Enot providedUncertain significance
(Dec 8, 2017)
criteria provided, single submitterVCV000618227
6.
GRCh37:
Chr17:8380201
GRCh38:
Chr17:8476883
MYH10R1958W, R1927W, R1936W, R1937Wnot providedUncertain significance
(Nov 9, 2017)
criteria provided, single submitterVCV000618226
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