Variant #0000001143 (NC_000011.9:g.5247993_5247996delCTTT)
Individual ID |
00000001, 00000008, 00000015, 00000018, 00000021, 00000022, 00000025, 00000026, 00000027, 00000028, 00000029, 00000030, 00000031, 00000072, 00000073, 00000074, 00000075, 00000076, 00000077, 00000081, 00000082, 00000084, 00000085, 00000091, 00000092, 00000094, 00000103, 00000109, 00000116, 00000120, 00000131, 00000145, 00000150, 00000171, 00000201, 00000213, 00000216, 00000220, 00000222, 00000230, 00000239, 00000240, 00000244, 00000245, 00000247, 00000248, 00000253, 00000257, 00000262, 00000263, 00000265, 00000266, 00000268, 00000273, 00000278, 00000283, 00000285, 00000286, 00000287, 00000290, 00000292, 00000293, 00000296, 00000301, 00000302, 00000304, 00000307, 00000308, 00000414, 00000416, 00000418, 00000421, 00000423, 00000424, 00000425, 00000427, 00000430, 00000433, 00000434, 00000448, 00000453, 00000454, 00000455, 00000458, 00000460 |
Chromosome |
11 |
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.5247993_5247996delCTTT |
Reference |
(OMIM 0326);dbSNP;Chen et al. |
DB-ID |
chr11_000206 |
Frequency |
- |
Variant remarks |
Codons 41/42 (-TTCT) |
ClassClinical |
Pathogenic |
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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