Variant #0000000101 (NC_000011.9:g.5270002G>A, HBG1(NM_000559.2):c.316-285C>T)

Individual ID 00000460, 00000913, 00001780, 00001965, 00001997
Chromosome 11
Allele Both (homozygous)
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Type Deletion
DNA change (genomic) (Relative to hg19 / GRCh37) g.5270002G>A
Reference GenBank;dbSNP
DB-ID HBG1_000003 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HBG1 NM_000559.2 ./. - c.316-285C>T r.(=) p.(=)



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000459 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2 49 Qi Ming
0000000912 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2 49 Qi Ming
0000001779 DNA SEQ-NG-I BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2, HBS1L, MYB 58 Qi Ming
0000001964 DNA SEQ-NG-I BCL11A, HBB, HBD, HBE1, HBG1, HBG2 47 Qi Ming
0000001996 DNA SEQ-NG-I BCL11A, HBA2, HBB, HBD, HBE1, HBG1, HBG2, HBS1L, MYB 59 Qi Ming