Hello everyone, I am trying to figure out about rs6165
(ref allele C and alt allele T/A/G) and rs6166
(ref allele C and alt allele T) variants.
When I go for the mRNA rs6165 (c.919G>A)
and I try to locate it shows A rather than getting a G.
and similarly, for rs6166
(c.2039G>A
) it shows T as a reference, on the transcript mrna (NM_000145.4)
.
The mutations are of the FSHR gene, is it because the gene is located on the negative strand? But still, I don't understand the purine and pyrimidine change. And all the literature survey on FSHR shows 919A>G
(instead of 919G>A
) and 2039A>G
(not 2039G>A
).
The chromosomal position shows C for both.
chromosomal location of rs6165 (Shows C)
chromosomal location of rs6166 (Shows C)
mRNA location of c.919G>A (Shows A)
mRNA location of c.2039G>A (Shows T)