Variant #0000305205 (NC_000021.8:g.47754510_47754548del, PCNT(NM_006031.5):c.467_505del)
Chromosome |
21 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47754510_47754548del |
DNA change (hg38) |
g.46334596_46334634del |
Published as |
PCNT(NM_006031.5):c.429_467del (p.(His156_Gln168del)), PCNT(NM_006031.5):c.467_505del (p.H156_Q168del), PCNT(NM_006031.6):c.467_505del (p.H156_Q16...) |
ISCN |
- |
DB-ID |
PCNT_000185 See all 3 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
0 |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Variant not found in online data sets |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |

Variant on transcripts
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