Variant #0000505427 (NC_000001.10:g.218607532G>C, NM_003238.3:c.619G>C (TGFB2))
| Chromosome |
1 |
| 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.218607532G>C |
| DNA change (hg38) |
g.218434190G>C |
| Published as |
TGFB2(NM_001135599.2):c.703G>C (p.(Val235Leu)), TGFB2(NM_001135599.3):c.703G>C (p.V235L), TGFB2(NM_001135599.4):c.703G>C (p.V235L), TGFB2(NM_00323...) |
| ISCN |
- |
| DB-ID |
TGFB2_000039 See all 5 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) |
0.0033 View details |
| Owner |
VKGL-NL_VUmc |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_VUmc |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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