TGFBR1 splice variants in ExAC


The table below lists the TGFBR1 splice variants found in the ExAC population database. Click on each variant for more details, including presence in the 1000 Genomes and Exome Sequencing Project databases, a breakdown by ethnic class and the variant's role in inherited cardiac disease. Use the form below to customise the variant selection. The table can be sorted by variant location, variant type or ExAC frequency.




No. Genomic coord. Variant (CDS) Variant (Protein) Variant Type ExAC frequencyPopulations*
1. 101911454 c.1387-8T>C splice site 0.00004218
2. 101891132 c.98-5T>C splice site 0.00003336
3. 101895028 c.574+7T>A splice site 0.00002490
4. 101894792 c.345A>G splice site 0.00002480
5. 101911453 c.1387-9_1387-7delTTC splice site 0.00002182
6. 101891131 c.98-6T>C splice site 0.00001669
7. 101891138 c.99G>A splice site 0.00001661
8. 101891385 c.343+3A>G splice site 0.00000847
9. 101891381 c.342T>G p.T114T splice site 0.00000844
10. 101891381 c.342T>A splice site 0.00000844
11. 101900135 c.575-6C>T splice site 0.00000836
12. 101891128 c.98-9_98-8delTT splice site 0.00000835
13. 101909933 c.1256-3C>T splice site 0.00000834
14. 101891138 c.99G>T splice site 0.00000830
15. 101895029 c.574+8A>G splice site 0.00000830
16. 101900378 c.805+7A>G splice site 0.00000829
17. 101895027 c.574+6_574+7delAT splice site 0.00000829
18. 101894783 c.344-8T>C splice site 0.00000829
19. 101894787 c.344-4T>G splice site 0.00000828
20. 101908896 c.1255+5A>G splice site 0.00000824

* This highlights the relative frequency of the variant in the ExAC populations - Non-Finnish European, African, East Asian, South Asian, American and Finnish. Higher frequencies are denoted by darker shades of green, variants absent in a population are coloured light gray.

Genomic coordinates refer to the GRCh37 release of the human genome.