Variant #0000338984 (NC_000011.9:g.88960984T>A, NC_000011.9(NM_000372.4):c.1037-7T>A (TYR))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.88960984T>A
DNA change (hg38) g.89227816T>A
Published as TYR(NM_000372.4):c.1037-7T>A, TYR(NM_000372.5):c.1037-7T>A
ISCN -
DB-ID TYR_000025 See all 43 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) 0.00097 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TYR NM_000372.4 +/. - c.1037-7T>A r.(=) p.(=)


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