Variant #0001038287 (NC_000011.9:g.120998747C>G, NM_005422.2:c.2061C>G (TECTA))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.120998747C>G
DNA change (hg38) -
Published as TECTA(NM_005422.2):c.2061C>G (p.N687K), TECTA(NM_005422.4):c.2061C>G (p.N687K)
ISCN -
DB-ID TECTA_000108 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00172 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TECTA NM_005422.2 -?/. - c.2061C>G r.(?) p.(Asn687Lys)


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