Transcript #00000091 (NM_000254.2, MTR gene)

Transcript name 5-methyltetrahydrofolate-homocysteine methyltransferase
Gene name MTR (5-methyltetrahydrofolate-homocysteine methyltransferase)
Chromosome 1
Transcript - NCBI ID NM_000254.2
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

220 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 00 c.-173G>A - -
./. 00 c.-151C>T - -
./. 00 c.-67C>T - -
./. 15 c.1348_1349TC>CA - p.Ser450His
./. 15 c.1348_1349TC>CA - p.Ser450His
./. 16 c.1516-93T>A, c.1516-93T>C - -
./. 01 c.34+45C>T - -
./. 01 c.34+151G>A - -
./. 02 c.35-21G>A - -
./. 02 c.155G>A - p.Arg52Gln
./. 02 c.185C>T - p.Pro62Leu
./. 02 c.249+244A>T - -
./. 04 c.340-166A>G - -
./. 04 c.340-166A>G - -
./. 04 c.340-6C>T - -
./. 04 c.381delA - p.Lys127LysfsX6
./. 04 c.409+74T>C - -
./. 04 c.409+79T>C - -
./. 04 c.409+113A>G - -
./. 05 c.410-155delA - -
./. 06 c.503-137T>C - -
./. 06 c.609+165A>G - -
./. 07 c.669+29_669+30ins4 - -
./. 07 c.669+32_669+33ins4 - -
./. 07 c.669+33T>G - -
./. 07 c.669+33_669+34ins4 - -
./. 08 c.670-195C>T - -
./. 08 c.670-152A>G - -
./. 08 c.670-148T>C - -
./. 08 c.685G>A - p.Val229Ile
./. 08 c.764+1G>C - -
./. 09 c.765-94A>C - -
./. 09 c.765-88T>G - -
./. 09 c.765-83G>A - -
./. 09 c.765-82A>G - -
./. 09 c.835A>C - p.Thr279Pro
./. 09 c.865+271G>T - -
./. 10 c.866-190_866-189ins9 - -
./. 10 c.866-187_866-186ins11 - -
./. 10 c.866-180_866-179ins11 - -
./. 10 c.866-44_866-43insT - -
./. 10 c.866-40_866-39insT - -
./. 10 c.866-39_866-38insT - -
./. 10 c.866-2A>C - -
./. 11 c.928-109G>A - -
./. 11 c.940G>A - p.Asp314Asn
./. 11 c.940G>A - p.Asp314Asn
./. 11 c.995+380delT - -
./. 12 c.996-195A>G - -
./. 12 c.996-160A>G - -
./. 12 c.1035T>C - p.Val345Val
./. 12 c.1075+185A>C - -
./. 13 c.1076-14_1076-15delGC - -
./. 14 c.1228G>C - p.Ala410Pro
./. 14 c.1298A>C - p.Asn433Thr
./. 14 c.1310C>A - p.Ser437Tyr
./. 14 c.1329+175G>T - -
./. 15 c.1330-169A>G - -
./. 15 c.1330-141T>G - -
./. 15 c.1437C>T - p.Asp479Asp
./. 15 c.1501G>T - p.Asp501Tyr
./. 15 c.1515+27A>G - -
./. 15 c.1515+103A>C - -
./. 15 c.1515+104T>C - -
./. 15 c.1515+133A>C - -
./. 15 c.1515+195_1515+196insC - -
./. 16 c.1516-88delT - -
./. 16 c.1516-51T>G - -
./. 16 c.1695+92_1695+94del3 - -
./. 16 c.1695+94A>C - -
./. 16 c.1695+95_1695+97del3 - -
./. 16 c.1695+96G>T - -
./. 16 c.1695+164G>T - -
./. 17 c.1696-193C>T - -
./. 17 c.1753C>T - p.Arg585X
./. 17 c.1784A>C - p.His595Pro
./. 17 c.1812+21G>A - -
./. 17 c.1812+91G>T - -
./. 18 c.1813-137G>A - -
./. 18 c.1813-103A>G - -
./. 18 c.1853_1854insC - -
./. 18 c.1862A>G - p.Asp621Gly
./. 19 c.2043+172A>G - -
./. 20 c.2044-196_2044-195insG - -
./. 20 c.2044-21T>C - -
./. 20 c.2044-17_2044-16insT - -
./. 20 c.2044-12_2044-11insT - -
./. 20 c.2044-11G>T - -
./. 20 c.2044-9C>T - -
./. 20 c.2045G>A - p.Gly682Asp
./. 20 c.2101delT - p.Tyr701IlefsX7
./. 20 c.2114_2115delTC - P.Leu705HisfsX4
./. 20 c.2114_2115delTC - P.Leu705HisfsX4
./. 20 c.2196+177G>C - -
./. 21 c.2197-183A>G - -
./. 21 c.2197-161G>T - -
./. 21 c.2230G>C - p.Val744Leu
./. 21 c.2234G>C - p.Gly745Ala
./. 21 c.2304+102T>C - -
./. 21 c.2304+149C>T - -
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