Variant #0000000069 (NC_000006.11:g.135424179C>G)
Individual ID |
00000001, 00000004, 00000007, 00000008, 00000018, 00000026, 00000031, 00000032, 00000033, 00000034, 00000036, 00000038, 00000039, 00000041, 00000043, 00000045, 00000050, 00000051, 00000053, 00000056, 00000065, 00000066, 00000068, 00000071, 00000072, 00000075, 00000079, 00000080, 00000081, 00000084, 00000089, 00000098, 00000100, 00000102, 00000103, 00000104, 00000105, 00000109, 00000110, 00000111, 00000119, 00000121, 00000122, 00000123, 00000126, 00000133, 00000136, 00000143, 00000147, 00000149, 00000151, 00000153, 00000156, 00000161, 00000162, 00000163, 00000165, 00000173, 00000174, 00000176, 00000177, 00000178, 00000179, 00000181, 00000182, 00000186, 00000188, 00000195, 00000200, 00000201, 00000206, 00000207, 00000214, 00000219, 00000222, 00000223, 00000226, 00000236, 00000240, 00000241, 00000243, 00000249, 00000251, 00000252, 00000263 |
Chromosome |
6 |
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.135424179C>G |
Reference |
GenBank;dbSNP |
DB-ID |
HBS1L_000003 See all 3 reported entries |
Frequency |
- |
Variant remarks |
- |
ClassClinical |
Likely benign |
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
|
|