Transcript #00029115 (NM_015448.1, DPCD gene)

Transcript name Manually created transcript
Gene name DPCD (deleted in primary ciliary dyskinesia homolog (mouse))
Chromosome 10
Transcript - NCBI ID NM_015448.1
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

42 entries on 1 page. Showing entries 1 - 42.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-3505T>G -3505 r.(=) p.(=) - utr-5 -
./. - c.-2153_-2149del -2153 r.(=) p.(=) - utr-5 -
./. - c.-2153_-2149del -2153 r.(=) p.(=) - utr-5 -
./. - c.-2153_-2149del -2153 r.(=) p.(=) - utr-5 -
./. - c.-2153_-2149del -2153 r.(=) p.(=) - utr-5 -
./. - c.-2153_-2149del -2153 r.(=) p.(=) - utr-5 -
./. - c.-2153_-2149del -2153 r.(=) p.(=) - utr-5 -
./. - c.-2153_-2149del -2153 r.(=) p.(=) - utr-5 -
./. - c.-2153_-2149del -2153 r.(=) p.(=) - utr-5 -
./. - c.-2153_-2149del -2153 r.(=) p.(=) - utr-5 -
./. - c.64+39C>T 64 r.(=) p.(=) - intron 39
./. - c.271-22G>A 271 r.(=) p.(=) - intron 22
./. - c.271-22G>A 271 r.(=) p.(=) - intron 22
./. - c.399C>T 399 r.(?) p.(=) - coding-synonymous -
./. - c.399C>T 399 r.(?) p.(=) - coding-synonymous -
./. - c.399C>T 399 r.(?) p.(=) - coding-synonymous -
./. - c.399C>T 399 r.(?) p.(=) - coding-synonymous -
./. - c.399C>T 399 r.(?) p.(=) - coding-synonymous -
./. - c.399C>T 399 r.(?) p.(=) - coding-synonymous -
./. - c.399C>T 399 r.(?) p.(=) - coding-synonymous -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.467T>C 467 r.(?) p.(Leu156Ser) - missense -
./. - c.*1813C>G 2425 r.(=) p.(=) - utr-3 -
./. - c.*1813C>G 2425 r.(=) p.(=) - utr-3 -
./. - c.*1813C>G 2425 r.(=) p.(=) - utr-3 -
./. - c.*1813C>G 2425 r.(=) p.(=) - utr-3 -
./. - c.*1813C>G 2425 r.(=) p.(=) - utr-3 -
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