Variant #0000619869 (NC_000023.10:g.71813117C>G, NM_001122670.1:c.3041G>C (PHKA1))
Chromosome |
X |
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.71813117C>G |
DNA change (hg38) |
g.72593267C>G |
Published as |
PHKA1(NM_002637.3):c.3080G>C (p.G1027A), PHKA1(NM_002637.4):c.3080G>C (p.(Gly1027Ala), p.G1027A) |
ISCN |
- |
DB-ID |
PHKA1_000011 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 |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
3.0E-5 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-12-04 15:24:38 +01:00 (CET) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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