Variant #0000860192 (NC_000006.11:g.146480775_146480778del, GRM1(NM_001278064.1):c.950+42_950+45del)
Chromosome |
6 |
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.146480775_146480778del |
DNA change (hg38) |
- |
Published as |
GRM1(NM_000838.3):c.950+14_950+17del (p.?), GRM1(NM_001278064.2):c.950+42_950+45delTCTC, GRM1(NM_001278065.2):c.950+42_950+45delTCTC |
ISCN |
- |
DB-ID |
GRM1_000044 See all 3 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_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |

Variant on transcripts
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