Variant #0000568812 (NC_000019.9:g.7600836C>T, NM_006702.4:c.45C>T (PNPLA6))
Chromosome |
19 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.7600836C>T |
DNA change (hg38) |
g.7535950C>T |
Published as |
PNPLA6(NM_001166111.1):c.189C>T (p.I63=), PNPLA6(NM_001166111.2):c.189C>T (p.I63=), PNPLA6(NM_006702.5):c.45C>T (p.I15=) |
ISCN |
- |
DB-ID |
MCOLN1_000027 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) |
0.00064 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 |
2022-11-01 13:01:21 +01:00 (CET) |

Variant on transcripts
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