Variant #0000889665 (NC_000011.9:g.119214515G>C, NC_000011.9(NM_031433.2):c.1124+11C>G (MFRP))
Chromosome |
11 |
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.119214515G>C |
DNA change (hg38) |
- |
Published as |
C1QTNF5(NM_015645.5):c.-1513+11C>G, MFRP(NM_031433.4):c.1124+11C>G |
ISCN |
- |
DB-ID |
C1QTNF5_000088 |
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) |
0.00297 View details |
Owner |
VKGL-NL_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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