Variant #0000001116 (NC_000016.9:g.215400_234700del)
Individual ID |
00000003, 00000009, 00000039, 00000040, 00000042, 00000043, 00000046, 00000047, 00000048, 00000049, 00000051, 00000054, 00000055, 00000056, 00000057, 00000058, 00000059, 00000061, 00000063, 00000069, 00000070, 00000077, 00000079, 00000081, 00000086, 00000087, 00000088, 00000089, 00000090, 00000093, 00000094, 00000098, 00000099, 00000100, 00000101, 00000102, 00000105, 00000107, 00000108, 00000111, 00000112, 00000113, 00000119, 00000122, 00000124, 00000126, 00000127, 00000128, 00000129, 00000130, 00000132, 00000133, 00000134, 00000137, 00000139, 00000140, 00000141, 00000142, 00000143, 00000146, 00000147, 00000149, 00000151, 00000152, 00000154, 00000157, 00000158, 00000160, 00000161, 00000162, 00000163, 00000164, 00000165, 00000167, 00000168, 00000169, 00000170, 00000172, 00000173, 00000175, 00000176, 00000177, 00000192, 00000193, 00000194 |
Chromosome |
16 |
Allele |
Parent #1 |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Deletion |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.215400_234700del |
Reference |
Xu et al |
DB-ID |
chr16_000013 |
Frequency |
- |
Variant remarks |
- -SEA |
ClassClinical |
Pathogenic |
Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |
Variant on transcripts
Screenings
|
|