Variant #0000311835 (NC_000011.9:g.2186495G>C, INS(NM_000207.2):c.-4115C>G)
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
VUS |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2186495G>C |
DNA change (hg38) |
g.2165265G>C |
Published as |
TH(NM_199292.3):c.1394C>G (p.S465C) |
ISCN |
- |
DB-ID |
TH_000006 |
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) |
2.0E-5 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |

Variant on transcripts
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