Variant #0000332780 (NC_000009.11:g.124062405G>T, NC_000009.11(NM_000177.4):c.144+122G>T (GSN))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.124062405G>T
DNA change (hg38) g.121300127G>T
Published as GSN(NM_000177.4):c.144+122G>T (p.(=)), GSN(NM_001127663.2):c.100-1836G>T
ISCN -
DB-ID GSN_000005 See all 2 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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GSN NM_000177.4 ?/. - c.144+122G>T r.(=) p.(=)


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