Variant #0000560372 (NC_000017.10:g.16220000T>C, NM_004278.3:c.500T>C (PIGL))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.16220000T>C |
DNA change (hg38) |
g.16316686T>C |
Published as |
PIGL(NM_004278.3):c.500T>C (p.L167P, p.(Leu167Pro)), PIGL(NM_004278.4):c.500T>C (p.L167P) |
ISCN |
- |
DB-ID |
PIGL_000002 See all 12 reported entries |
Variant remarks |
VKGL data sharing initiative Nederland |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
CLASSIFICATION record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
0.00042 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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