S I D E B A R
Format
Items per page
Sort by

Download:

Choose Destination

Search results

Items: 1 to 100 of 474

VariationLocationGene(s)Protein changeCondition(s)Clinical significance
(Last reviewed)
Review statusAccession
1.
GRCh37:
Chr2:96915962
GRCh38:
Chr2:96250224
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000897611
2.
GRCh37:
Chr2:96915977
GRCh38:
Chr2:96250239
TMEM127PheochromocytomaBenign
(Jan 12, 2018)
criteria provided, single submitterVCV000337444
3.
GRCh37:
Chr2:96915978
GRCh38:
Chr2:96250240
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337445
4.
GRCh37:
Chr2:96915986
GRCh38:
Chr2:96250248
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337446
5.
GRCh37:
Chr2:96916150
GRCh38:
Chr2:96250412
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000897612
6.
GRCh37:
Chr2:96916155
GRCh38:
Chr2:96250417
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000897613
7.
GRCh37:
Chr2:96916198
GRCh38:
Chr2:96250460
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000337447
8.
GRCh37:
Chr2:96916275
GRCh38:
Chr2:96250537
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000897614
9.
GRCh37:
Chr2:96916337
GRCh38:
Chr2:96250599
TMEM127PheochromocytomaBenign
(Jan 12, 2018)
criteria provided, single submitterVCV000337448
10.
GRCh37:
Chr2:96916338-96916340
GRCh38:
Chr2:96250600-96250602
TMEM127PheochromocytomaLikely benign
(Jun 14, 2016)
criteria provided, single submitterVCV000337449
11.
GRCh37:
Chr2:96916412
GRCh38:
Chr2:96250674
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337450
12.
GRCh37:
Chr2:96916497
GRCh38:
Chr2:96250759
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000898770
13.
GRCh37:
Chr2:96916521
GRCh38:
Chr2:96250783
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337451
14.
GRCh37:
Chr2:96916580
GRCh38:
Chr2:96250842
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000337452
15.
GRCh37:
Chr2:96916635
GRCh38:
Chr2:96250897
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000898771
16.
GRCh37:
Chr2:96916658
GRCh38:
Chr2:96250920
TMEM127PheochromocytomaLikely benign
(Jun 14, 2016)
criteria provided, single submitterVCV000337453
17.
GRCh37:
Chr2:96916671
GRCh38:
Chr2:96250933
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000898772
18.
GRCh37:
Chr2:96916686
GRCh38:
Chr2:96250948
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000898773
19.
GRCh37:
Chr2:96916701
GRCh38:
Chr2:96250963
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000337454
20.
GRCh37:
Chr2:96916746
GRCh38:
Chr2:96251008
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000895800
21.
GRCh37:
Chr2:96916786
GRCh38:
Chr2:96251048
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337455
22.
GRCh37:
Chr2:96916827
GRCh38:
Chr2:96251089
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000337456
23.
GRCh37:
Chr2:96916829
GRCh38:
Chr2:96251091
TMEM127PheochromocytomaUncertain significance
(Jun 14, 2016)
criteria provided, single submitterVCV000337457
24.
GRCh37:
Chr2:96916862
GRCh38:
Chr2:96251124
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000895801
25.
GRCh37:
Chr2:96916904
GRCh38:
Chr2:96251166
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337458
26.
GRCh37:
Chr2:96916983
GRCh38:
Chr2:96251245
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000895802
27.
GRCh37:
Chr2:96916998
GRCh38:
Chr2:96251260
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000337459
28.
GRCh37:
Chr2:96917028
GRCh38:
Chr2:96251290
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000896085
29.
GRCh37:
Chr2:96917043
GRCh38:
Chr2:96251305
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337460
30.
GRCh37:
Chr2:96917048
GRCh38:
Chr2:96251310
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000337461
31.
GRCh37:
Chr2:96917101
GRCh38:
Chr2:96251363
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337462
32.
GRCh37:
Chr2:96917135
GRCh38:
Chr2:96251397
TMEM127PheochromocytomaUncertain significance
(Apr 27, 2017)
criteria provided, single submitterVCV000896086
33.
GRCh37:
Chr2:96917246
GRCh38:
Chr2:96251508
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000337463
34.
GRCh37:
Chr2:96917247
GRCh38:
Chr2:96251509
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000896087
35.
GRCh37:
Chr2:96917254-96917255
GRCh38:
Chr2:96251516-96251517
TMEM127PheochromocytomaUncertain significance
(Jun 14, 2016)
criteria provided, single submitterVCV000337464
36.
GRCh37:
Chr2:96917275-96917276
GRCh38:
Chr2:96251537-96251538
TMEM127PheochromocytomaUncertain significance
(Jun 14, 2016)
criteria provided, single submitterVCV000337465
37.
GRCh37:
Chr2:96917301
GRCh38:
Chr2:96251563
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337466
38.
GRCh37:
Chr2:96917375
GRCh38:
Chr2:96251637
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000337467
39.
GRCh37:
Chr2:96917418
GRCh38:
Chr2:96251680
TMEM127PheochromocytomaUncertain significance
(Apr 27, 2017)
criteria provided, single submitterVCV000897674
40.
GRCh37:
Chr2:96917425
GRCh38:
Chr2:96251687
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000337468
41.
GRCh37:
Chr2:96917443-96917445
GRCh38:
Chr2:96251705-96251707
TMEM127PheochromocytomaLikely benign
(Jun 14, 2016)
criteria provided, single submitterVCV000337469
42.
GRCh37:
Chr2:96917460
GRCh38:
Chr2:96251722
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000337470
43.
GRCh37:
Chr2:96917534
GRCh38:
Chr2:96251796
TMEM127PheochromocytomaBenign
(Jan 12, 2018)
criteria provided, single submitterVCV000337471
44.
GRCh37:
Chr2:96917588
GRCh38:
Chr2:96251850
TMEM127PheochromocytomaBenign
(Jan 12, 2018)
criteria provided, single submitterVCV000337472
45.
GRCh37:
Chr2:96917659-96917660
GRCh38:
Chr2:96251921-96251922
TMEM127PheochromocytomaUncertain significance
(Jun 14, 2016)
criteria provided, single submitterVCV000337473
46.
GRCh37:
Chr2:96917667
GRCh38:
Chr2:96251929
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000897675
47.
GRCh37:
Chr2:96917697
GRCh38:
Chr2:96251959
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337474
48.
GRCh37:
Chr2:96917724
GRCh38:
Chr2:96251986
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000898839
49.
GRCh37:
Chr2:96917727
GRCh38:
Chr2:96251989
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337476
50.
GRCh37:
Chr2:96917727
GRCh38:
Chr2:96251989
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337475
51.
GRCh37:
Chr2:96917762
GRCh38:
Chr2:96252024
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337477
52.
GRCh37:
Chr2:96917774
GRCh38:
Chr2:96252036
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000337478
53.
GRCh37:
Chr2:96917823
GRCh38:
Chr2:96252085
TMEM127PheochromocytomaBenign
(Jan 12, 2018)
criteria provided, single submitterVCV000337479
54.
GRCh37:
Chr2:96917908
GRCh38:
Chr2:96252170
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000337480
55.
GRCh37:
Chr2:96917926
GRCh38:
Chr2:96252188
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337481
56.
GRCh37:
Chr2:96918041
GRCh38:
Chr2:96252303
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000895877
57.
GRCh37:
Chr2:96918140
GRCh38:
Chr2:96252402
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337482
58.
GRCh37:
Chr2:96918240
GRCh38:
Chr2:96252502
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000337483
59.
GRCh37:
Chr2:96918245
GRCh38:
Chr2:96252507
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000337484
60.
GRCh37:
Chr2:96918289
GRCh38:
Chr2:96252551
TMEM127PheochromocytomaUncertain significance
(Apr 27, 2017)
criteria provided, single submitterVCV000895878
61.
GRCh37:
Chr2:96918294
GRCh38:
Chr2:96252556
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000337485
62.
GRCh37:
Chr2:96918313
GRCh38:
Chr2:96252575
TMEM127PheochromocytomaBenign
(Jan 13, 2018)
criteria provided, single submitterVCV000337486
63.
GRCh37:
Chr2:96918349
GRCh38:
Chr2:96252611
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337487
64.
GRCh37:
Chr2:96918368
GRCh38:
Chr2:96252630
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337488
65.
GRCh37:
Chr2:96918383
GRCh38:
Chr2:96252645
TMEM127PheochromocytomaBenign
(Jan 12, 2018)
criteria provided, single submitterVCV000337489
66.
GRCh37:
Chr2:96918566
GRCh38:
Chr2:96252828
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000896151
67.
GRCh37:
Chr2:96918566
GRCh38:
Chr2:96252828
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337490
68.
GRCh37:
Chr2:96918663
GRCh38:
Chr2:96252925
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337491
69.
GRCh37:
Chr2:96918680
GRCh38:
Chr2:96252942
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000896152
70.
GRCh37:
Chr2:96918785-96918786
GRCh38:
Chr2:96253047-96253048
TMEM127PheochromocytomaUncertain significance
(Jun 14, 2016)
criteria provided, single submitterVCV000337492
71.
GRCh37:
Chr2:96918786
GRCh38:
Chr2:96253048
TMEM127PheochromocytomaLikely benign
(Jun 14, 2016)
criteria provided, single submitterVCV000337493
72.
GRCh37:
Chr2:96918871-96918872
GRCh38:
Chr2:96253133-96253134
TMEM127PheochromocytomaLikely benign
(Jun 14, 2016)
criteria provided, single submitterVCV000337494
73.
GRCh37:
Chr2:96918884
GRCh38:
Chr2:96253146
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000337495
74.
GRCh37:
Chr2:96918934
GRCh38:
Chr2:96253196
TMEM127PheochromocytomaUncertain significance
(Jan 12, 2018)
criteria provided, single submitterVCV000897751
75.
GRCh37:
Chr2:96919044
GRCh38:
Chr2:96253306
TMEM127PheochromocytomaBenign
(Jan 12, 2018)
criteria provided, single submitterVCV000337496
76.
GRCh37:
Chr2:96919206
GRCh38:
Chr2:96253468
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000897752
77.
GRCh37:
Chr2:96919208
GRCh38:
Chr2:96253470
TMEM127PheochromocytomaBenign
(Jan 12, 2018)
criteria provided, single submitterVCV000337497
78.
GRCh37:
Chr2:96919297
GRCh38:
Chr2:96253559
TMEM127PheochromocytomaUncertain significance
(Jun 14, 2016)
criteria provided, single submitterVCV000337498
79.
GRCh37:
Chr2:96919367
GRCh38:
Chr2:96253629
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000897753
80.
GRCh37:
Chr2:96919489
GRCh38:
Chr2:96253751
TMEM127PheochromocytomaBenign
(Jan 12, 2018)
criteria provided, single submitterVCV000337499
81.
GRCh37:
Chr2:96919496
GRCh38:
Chr2:96253758
TMEM127not provided, PheochromocytomaBenign/Likely benign
(Jun 22, 2018)
criteria provided, multiple submitters, no conflictsVCV000337500
82.
GRCh37:
Chr2:96919530
GRCh38:
Chr2:96253792
TMEM127PheochromocytomaUncertain significance
(Jan 13, 2018)
criteria provided, single submitterVCV000897754
83.
GRCh37:
Chr2:96919551
GRCh38:
Chr2:96253813
TMEM127P238THereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Jul 10, 2018)
criteria provided, single submitterVCV000575095
84.
GRCh37:
Chr2:96919563
GRCh38:
Chr2:96253825
TMEM127P234THereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Oct 29, 2019)
criteria provided, single submitterVCV000953758
85.
GRCh37:
Chr2:96919563
GRCh38:
Chr2:96253825
TMEM127P234AHereditary cancer-predisposing syndrome, Hereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Apr 6, 2020)
criteria provided, multiple submitters, no conflictsVCV000826772
86.
GRCh37:
Chr2:96919569
GRCh38:
Chr2:96253831
TMEM127P232SHereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Sep 27, 2019)
criteria provided, single submitterVCV000942472
87.
GRCh37:
Chr2:96919570
GRCh38:
Chr2:96253832
TMEM127Q231HHereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Jul 25, 2019)
criteria provided, single submitterVCV000962522
88.
GRCh37:
Chr2:96919573
GRCh38:
Chr2:96253835
TMEM127Hereditary Paraganglioma-Pheochromocytoma SyndromesLikely benign
(Mar 13, 2019)
criteria provided, single submitterVCV001088175
89.
GRCh37:
Chr2:96919573
GRCh38:
Chr2:96253835
TMEM127F230LHereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Mar 20, 2019)
criteria provided, single submitterVCV000837449
90.
GRCh37:
Chr2:96919584
GRCh38:
Chr2:96253846
TMEM127I227FHereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Sep 21, 2019)
criteria provided, single submitterVCV000960226
91.
GRCh37:
Chr2:96919589
GRCh38:
Chr2:96253851
TMEM127E225GHereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Oct 3, 2019)
criteria provided, single submitterVCV000935490
92.
GRCh37:
Chr2:96919591
GRCh38:
Chr2:96253853
TMEM127Hereditary cancer-predisposing syndrome, Hereditary Paraganglioma-Pheochromocytoma SyndromesLikely benign
(Oct 26, 2020)
criteria provided, multiple submitters, no conflictsVCV000413245
93.
GRCh37:
Chr2:96919592
GRCh38:
Chr2:96253854
TMEM127Y224CHereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Dec 4, 2016)
criteria provided, single submitterVCV000405197
94.
GRCh37:
Chr2:96919594
GRCh38:
Chr2:96253856
TMEM127E223DHereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Jul 15, 2018)
criteria provided, single submitterVCV000655845
95.
GRCh37:
Chr2:96919596
GRCh38:
Chr2:96253858
TMEM127E223KHereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Aug 26, 2020)
criteria provided, single submitterVCV000532524
96.
GRCh37:
Chr2:96919597
GRCh38:
Chr2:96253859
TMEM127Hereditary cancer-predisposing syndrome, Hereditary Paraganglioma-Pheochromocytoma SyndromesLikely benign
(Dec 3, 2020)
criteria provided, multiple submitters, no conflictsVCV000413237
97.
GRCh37:
Chr2:96919598
GRCh38:
Chr2:96253860
TMEM127A222VHereditary cancer-predisposing syndrome, Hereditary Paraganglioma-Pheochromocytoma SyndromesConflicting interpretations of pathogenicity
(May 18, 2020)
criteria provided, conflicting interpretationsVCV000405200
98.
GRCh37:
Chr2:96919600
GRCh38:
Chr2:96253862
TMEM127Hereditary cancer-predisposing syndrome, Hereditary Paraganglioma-Pheochromocytoma SyndromesLikely benign
(Dec 1, 2020)
criteria provided, multiple submitters, no conflictsVCV000463855
99.
GRCh37:
Chr2:96919601
GRCh38:
Chr2:96253863
TMEM127P221LHereditary cancer-predisposing syndrome, Hereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Aug 20, 2018)
criteria provided, multiple submitters, no conflictsVCV000648969
100.
GRCh37:
Chr2:96919605
GRCh38:
Chr2:96253867
TMEM127Y220HHereditary Paraganglioma-Pheochromocytoma SyndromesUncertain significance
(Mar 10, 2020)
criteria provided, single submitterVCV001014859
Format
Items per page
Sort by

Download:

Choose Destination
Support Center