Variant #0000559139 (NC_000016.9:g.75669656A>C, NM_005548.2:c.717T>G (KARS))
Chromosome |
16 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.75669656A>C |
DNA change (hg38) |
g.75635758A>C |
Published as |
KARS(NM_001130089.1):c.801T>G (p.F267L), KARS(NM_005548.3):c.717T>G (p.(Phe239Leu)), KARS1(NM_001130089.2):c.801T>G (p.F267L) |
ISCN |
- |
DB-ID |
KARS_000022 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) |
0.00079 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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