Variant #0000558410 (NC_000016.9:g.51175683_51175685dup, NM_002968.2:c.475_477dup (SALL1))
Chromosome |
16 |
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.51175683_51175685dup |
DNA change (hg38) |
g.51141772_51141774dup |
Published as |
SALL1(NM_001127892.1):c.178_180dup (p.(Ser62dup)), SALL1(NM_001127892.2):c.184_186dupAGC (p.S62dup), SALL1(NM_002968.2):c.475_477dupAGC (p.S159dup) |
ISCN |
- |
DB-ID |
SALL1_000080 See all 4 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 |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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