Variant #0000000056 (NC_000011.9:g.5294135delT)
Individual ID |
00000003, 00000004, 00000005, 00000006, 00000009, 00000010, 00000016, 00000018, 00000020, 00000021, 00000023, 00000025, 00000026, 00000027, 00000031, 00000032, 00000035, 00000036, 00000037, 00000042, 00000044, 00000045, 00000048, 00000050, 00000054, 00000063, 00000064, 00000066, 00000069, 00000072, 00000073, 00000074, 00000077, 00000080, 00000082, 00000086, 00000088, 00000090, 00000095, 00000099, 00000100, 00000101, 00000106, 00000109, 00000110, 00000111, 00000112, 00000115, 00000119, 00000120, 00000121, 00000122, 00000123, 00000125, 00000130, 00000132, 00000136, 00000139, 00000140, 00000142, 00000143, 00000146, 00000147, 00000151, 00000162, 00000163, 00000169, 00000170, 00000173, 00000181, 00000184, 00000186, 00000188, 00000189, 00000195, 00000197, 00000198, 00000201, 00000204, 00000210, 00000211, 00000212, 00000213, 00000214, 00000217 |
Chromosome |
11 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Substitution |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.5294135delT |
Reference |
GenBank |
DB-ID |
HBE1_000008 See all 2 reported entries |
Frequency |
- |
Variant remarks |
- |
ClassClinical |
uncertain significance |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
Screenings
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