View unique variants - Diamond-Blackfan Anemia - Leiden Open Variation Database

About this overview [Show]

The variants below are all in the RPS26 database. In this view only variant fields are shown. Variants are listed only once, a number is present in the DNA change field when a variant has been reported more than once (in such cases fields other than the DNA change just belong to one entry and may differ for other entries).
Selecting and clicking a specific line will open a detailed view showing all variant entries, including patient and pathogenicity information.
At the bottom of this page a legend is provided with a short explanation of what each field contains.
For a more detailed description of each field, please see the RPS26 full legend here.

8 entries
entries per page

Exon

DNA change

RNA change

Protein

Frequency

DB-ID

Location

Remarks

Molecula Mechanisms


01	c.1A>G (Reported 6 times)	-	p.Met1Val	-	RPS26_00002	-	Missense mutation	transition
01	c.1A>T	-	p.Met1Leu	-	RPS26_00001	-	Missense mutation	transversion
01	c.1T>G	-	p.Met1Arg	-	RPS26_00003	-	Missense mutation	transversion
01	c.3+1G>A	-	p.0?	-	RPS26_00007	Intron 1	Donor splice site defect	transition
01	c.3+1G>C	-	p.0?	-	RPS26_00006	Intron 1	Donor splice site defect	transversion
02	c.3+1G>T	-	p.0?	-	RPS26_00008	Intron 1	Donor splice site defect	transversion
02	c.31 32insG	-	p.Ala11GlyfsX15	-	RPS26_00005	-	Insertion	slippage
02	c.97G>A	-	p.Asp33Asn	-	RPS26_00004	-	Missense mutation	transition

1 - 8

Legend: [ RPS26 full legend ]
Sequence variations are described basically as recommended by the Ad-Hoc Committee for Mutation Nomenclature (AHCMN), with the recently suggested additions (den Dunnen JT and Antonarakis SE [2000], Hum.Mut. 15:7-12); for a summary see Nomenclature. Coding DNA Reference Sequence, with the first base of the Met-codon counted as position 1.
Exon: Exon numbering. DNA change: Variation at DNA-level. If present, "Full Details" will show you the the full-length entry. RNA change: Variation at RNA-level, (?) unknown but probably identical to DNA. Protein: Variation at protein level. Frequency: Frequency of polymorphism. RPS26 DB-ID: Database IDentifier; When available, links to OMIM ID's are provided. Location: Variant location at DNA level. Remarks: Description of the variant Molecula Mechanisms: Molecular mechanisms

Diamond-Blackfan Anemia

ribosomal protein S26 (RPS26)