Variant #0000546293 (NC_000012.11:g.103352200_103352208dup, NM_004316.3:c.178_186dup (ASCL1))
Chromosome |
12 |
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.103352200_103352208dup |
DNA change (hg38) |
g.102958422_102958430dup |
Published as |
ASCL1(NM_004316.3):c.178_186dupCAGCAGCAG (p.Q60_Q62dup), ASCL1(NM_004316.4):c.178_186dupCAGCAGCAG (p.Q60_Q62dup), PAH(NM_001354304.2):c.-303_-295du... |
ISCN |
- |
DB-ID |
ASCL1_000015 See all 2 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) |
Retrieve |
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 |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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