Variant #0000441390 (NC_000006.11:g.7542226G>T, DSP(NM_004415.2):c.78G>T)
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Does not affect function |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.7542226G>T |
DNA change (hg38) |
g.7541993G>T |
Published as |
- |
ISCN |
- |
DB-ID |
DSP_000153 See all 2 reported entries |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
rs71559180 |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
6.0E-5 View details |
Owner |
Paul van der Zwaag |
Database submission license |
No license selected |
Created by |
Paul van der Zwaag |
Date created |
2009-09-01 15:30:32 +02:00 (CEST) |
Date last edited |
2018-12-24 13:09:58 +01:00 (CET) |

Variant on transcripts
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