Deletion#
Deletion: a sequence change where, compared to a reference sequence, one or more nucleotides are not present (deleted).
Syntax#
Syntax | sequence_identifier ":r." position "del" |
---|---|
Examples |
|
Explanation of Symbols | |
|
Notes#
- all variants should be described on the DNA level; descriptions on the RNA and/or protein level may be given in addition.
position(s)_deleted
should contain two different positions, e.g.,123_126
, not123_123
.- the
position(s)_deleted
should be listed from 5' to 3', e.g.,123_126
, not126_123
. - for all descriptions, the most 3' position possible of the reference sequence is arbitrarily assigned to have been changed (3'rule).
- the 3'rule also applies for changes in single residue stretches and tandem repeats (nucleotide or amino acid).
NOTE: the exception to the 3'rule for deletions around exon/exon junctions (see Deletions) does not apply when describing variants based on an RNA reference sequence.
- the 3'rule also applies for changes in single residue stretches and tandem repeats (nucleotide or amino acid).
- see Uncertain; when the position and/or the sequence of a deletion has not been defined, a description may have a format like
r.(100_150)delN[15]
.
Examples#
-
one nucleotide
LRG_199t1:r.10del
a deletion of theu
at positionr.10
in the reference sequenceLRG_199t1
.
-
several nucleotides
-
NM_004006.2:r.6_8del
a deletion of nucleotidesr.6
tor.8
in the reference sequenceNM_004006.2
.
NOTE: the recommendation is not to describe the variant asr.6_8deluug
, i.e., describe the deleted nucleotide sequence. -
LRG_2t1:r.1034_1036del
a deletion of nucleotidesr.1034
tor.1036
(uug
) in the reference sequenceLRG_2t1
.
NOTE: since the 3'rule has to be applied, the variant, crossing the intron between nucleotidesr.1035
andr.1036
, is not described asr.1033_1035del
(deletionguu
). -
LRG_199t1:r.(4072_5145del)
the predicted deletion of exon 30 (starting at positionr.4072
) to exon 36 (ending at positionr.5145
) of the DMD gene; RNA has not been analysed.
-
-
LRG_199t1:r.=/6_8del
a mosaic case where from positionr.6
tor.8
, besides the normal sequence, also transcripts are found containing a deletion of this sequence.
NOTE: for the predicted consequences of a variant, the description isLRG_199t1:r.(=/6_8del)
.
Discussion#
Can I use r.123del6
to describe a 6 nucleotide deletion?
No, a deletion of more than one residue should mention the first and last residue deleted, separated using the range symbol ("_", underscore), e.g., r.123_128del
and not r.123del6
.
Is the description of a deletion of exon 17 as r.EX17del
still allowed?
A description like r.EX17del
has never been allowed.
Descriptions should be specific and indicate the nucleotides affected by the change.