Variant #0000507648 (NC_000001.10:g.45797188_45797189dup, NM_001128425.1:c.1227_1228dup (MUTYH))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45797188_45797189dup |
DNA change (hg38) |
g.45331516_45331517dup |
Published as |
MUTYH(NM_001048171.1):c.1185_1186dup (p.(Glu396Glyfs*43)), MUTYH(NM_001128425.1):c.1227_1228dupGG (p.E410Gfs*43), MUTYH(NM_001128425.2):c.1227_1228... |
ISCN |
- |
DB-ID |
MUTYH_000078 See all 42 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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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