Variant #0000000001 (NC_000016.9:g.213795T>C)
Individual ID |
00000001, 00000007, 00000018, 00000020, 00000021, 00000030, 00000034, 00000036, 00000041, 00000044, 00000046, 00000050, 00000051, 00000052, 00000065, 00000066, 00000068, 00000073, 00000083, 00000088, 00000092, 00000093, 00000095, 00000098, 00000099, 00000102, 00000103, 00000109, 00000111, 00000117, 00000134, 00000155, 00000159, 00000168, 00000169, 00000181, 00000182, 00000185, 00000189, 00000190, 00000191, 00000199, 00000201, 00000211, 00000213, 00000214, 00000215, 00000219, 00000227, 00000236, 00000239, 00000240, 00000241, 00000242, 00000250, 00000251, 00000252, 00000264, 00000265, 00000266, 00000268, 00000275, 00000283, 00000285, 00000286, 00000288, 00000289, 00000290, 00000296, 00000300, 00000302, 00000309, 00000312, 00000313, 00000315, 00000316, 00000321, 00000325, 00000333, 00000335, 00000347, 00000350, 00000354, 00000359, 00000364 |
Chromosome |
16 |
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.213795T>C |
Reference |
GenBank;dbSNP |
DB-ID |
HBA2_000003 See all 4 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
|
|