Variant #0000268178 (NC_000001.10:g.103496816_103496818dup, NC_000001.10(NM_001854.3):c.652-8_652-6dup (COL11A1))
Chromosome |
1 |
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.103496816_103496818dup |
DNA change (hg38) |
g.103031260_103031262dup |
Published as |
COL11A1(NM_001190709.1):c.652-6_652-5insTTT (p.(=)), COL11A1(NM_001854.4):c.652-9_652-7dupTTT, COL11A1(NM_080629.2):c.652-8_652-6dupTTT, COL11A1(N...) |
ISCN |
- |
DB-ID |
COL11A1_000086 See all 5 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_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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