Transcript #00000530 (NM_153834.3, GPR112 gene)

Transcript name G protein-coupled receptor 112
Gene name GPR112 (G protein-coupled receptor 112)
Chromosome X
Transcript - NCBI ID NM_153834.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_722576.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

113 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.158G>A r.(?) p.(Ser53Asn)
?/. - c.178G>A r.(?) p.(Asp60Asn)
-?/. - c.325T>C r.(?) p.(Ser109Pro)
?/. - c.325T>C r.(?) p.(Ser109Pro)
?/. - c.331C>T r.(?) p.(Arg111Cys)
-?/. - c.340C>T r.(?) p.(Leu114=)
-?/. - c.477C>G r.(?) p.(Phe159Leu)
?/. - c.508G>A r.(?) p.(Glu170Lys)
-?/. - c.513T>C r.(?) p.(Val171=)
-?/. - c.588G>C r.(?) p.(Glu196Asp)
?/. - c.828A>G r.(?) p.(Ile276Met)
?/. - c.1103C>A r.(?) p.(Pro368His)
-?/. - c.1150G>A r.(?) p.(Val384Ile)
?/. - c.1285C>T r.(?) p.(Pro429Ser)
-?/. - c.1420A>C r.(?) p.(Ile474Leu)
-?/. - c.1474C>T r.(?) p.(Pro492Ser)
-?/. - c.1477T>C r.(?) p.(Leu493=)
-?/. - c.1519T>C r.(?) p.(Leu507=)
-?/. - c.1666A>T r.(?) p.(Thr556Ser)
?/. - c.1828C>T r.(?) p.(Gln610Ter)
?/. - c.1910G>A r.(?) p.(Gly637Asp)
-?/. - c.1963A>G r.(?) p.(Ile655Val)
-?/. - c.1963A>G r.(?) p.(Ile655Val)
?/. - c.1963A>G r.(?) p.(Ile655Val)
?/. - c.2017A>G r.(?) p.(Ile673Val)
?/. - c.2209G>T r.(?) p.(Ala737Ser)
?/. - c.2963C>T r.(?) p.(Thr988Met)
?/. - c.3209C>A r.(?) p.(Thr1070Asn)
-?/. - c.3252G>A r.(=) p.(=)
?/. - c.3365C>T r.(?) p.(Ala1122Val)
-?/. - c.3365C>T r.(?) p.(Ala1122Val)
-?/. - c.3495G>A r.(?) p.(Thr1165=)
-?/. - c.3604A>G r.(?) p.(Thr1202Ala)
?/. - c.3610A>T r.(?) p.(Thr1204Ser)
-?/. - c.3615A>G r.(?) p.(Thr1205=)
?/. - c.3638C>A r.(?) p.(Thr1213Asn)
?/. - c.3638C>A r.(?) p.(Thr1213Asn)
?/. - c.3638C>A r.(?) p.(Thr1213Asn)
?/. - c.3697T>C r.(?) p.(Ser1233Pro)
?/. - c.4179T>C r.(?) p.(=)
?/. - c.4179T>C r.(?) p.(=)
-?/. - c.4179T>C r.(=) p.(=)
?/. - c.4618T>C r.(?) p.(Ser1540Pro)
?/. - c.4618T>C r.(?) p.(Ser1540Pro)
?/. - c.4618T>C r.(?) p.(Ser1540Pro)
-?/. - c.4633C>G r.(?) p.(Pro1545Ala)
-?/. - c.4639T>A r.(?) p.(Cys1547Ser)
-?/. - c.4639T>A r.(?) p.(Cys1547Ser)
?/. - c.4639T>A r.(?) p.(Cys1547Ser)
-?/. - c.4928C>T r.(?) p.(Thr1643Met)
-?/. - c.4938C>G r.(=) p.(=)
-?/. - c.5147G>A r.(?) p.(Gly1716Asp)
-?/. - c.5174C>T r.(?) p.(Ser1725Phe)
?/. - c.5182A>C r.(?) p.(Thr1728Pro)
?/. - c.5371T>C r.(?) p.(Phe1791Leu)
?/. - c.5371T>C r.(?) p.(Phe1791Leu)
?/. - c.5371T>C r.(?) p.(Phe1791Leu)
?/. - c.5493C>T r.(?) p.(=)
?/. - c.5493C>T r.(?) p.(=)
-?/. - c.5493C>T r.(=) p.(=)
-?/. - c.5517A>G r.(=) p.(=)
-?/. - c.5575C>G r.(?) p.(Gln1859Glu)
?/. - c.5591C>T r.(?) p.(Pro1864Leu)
-?/. - c.5592A>G r.(?) p.(Pro1864=)
?/. - c.5617A>G r.(?) p.(Ser1873Gly)
?/. - c.6208C>T r.(?) p.(Arg2070*)
?/. - c.6557C>T r.(?) p.(Ser2186Phe)
-?/. - c.6656C>G r.(?) p.(Thr2219Ser)
?/. - c.6823-21del r.(=) p.(=)
?/. - c.6823-21del r.(=) p.(=)
-?/. - c.6832A>G r.(?) p.(Ile2278Val)
?/. - c.6927+64A>G r.(=) p.(=)
?/. - c.6927+64A>G r.(=) p.(=)
?/. - c.6927+215G>T r.(=) p.(=)
?/. - c.6927+215G>T r.(=) p.(=)
?/. - c.6928-325G>T r.(=) p.(=)
-?/. - c.7074A>G r.(?) p.(Thr2358=)
-?/. - c.7211C>G r.(?) p.(Thr2404Ser)
?/. - c.7211C>G r.(?) p.(Thr2404Ser)
?/. - c.7265C>T r.(?) p.(Ala2422Val)
?/. - c.7278-279T>C r.(=) p.(=)
-?/. - c.7332A>G r.(?) p.(Gln2444=)
-?/. - c.7558G>A r.(?) p.(Val2520Ile)
-?/. - c.7938C>T r.(=) p.(=)
?/. - c.7941C>A r.(?) p.(=)
?/. - c.7941C>A r.(?) p.(=)
-?/. - c.7941C>A r.(=) p.(=)
?/. - c.7965_7967del r.(?) p.(Asp2657del)
?/. - c.7965_7967del r.(?) p.(Asp2657del)
?/. - c.7969_7971del r.(?) p.(Asp2657del)
?/. - c.7969_7971del r.(?) p.(Asp2657del)
?/. - c.7969_7971del r.(?) p.(Asp2657del)
?/. - c.8102C>T r.(?) p.(Ser2701Leu)
-?/. - c.8144T>C r.(?) p.(Ile2715Thr)
-?/. - c.8231C>T r.(?) p.(Ala2744Val)
?/. - c.8271T>C r.(?) p.(=)
?/. - c.8271T>C r.(?) p.(=)
-?/. - c.8271T>C r.(=) p.(=)
?/. - c.8307-51del r.(=) p.(=)
-?/. - c.8434G>A r.(?) p.(Ala2812Thr)
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