Variant #0000969822 (NC_000019.9:g.47987412C>T, NM_007059.2:c.6G>A (KPTN))

Chromosome 19
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.47987412C>T
DNA change (hg38) -
Published as KPTN(NM_007059.4):c.6G>A (p.M2I)
ISCN -
DB-ID KPTN_000025
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) 7.0E-5 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 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NAPA NM_003827.3 ?/. - c.*4133G>A r.(=) p.(=)
KPTN NM_007059.2 ?/. - c.6G>A r.(?) p.(Met2Ile)


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