Variant #0001002590 (NC_000016.9:g.75682511C>T, NM_005548.2:c.-974G>A (KARS))

Chromosome 16
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.75682511C>T
DNA change (hg38) -
Published as TERF2IP(NM_018975.3):c.670+61C>T
ISCN -
DB-ID KARS_000096
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) 6.0E-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 2024-08-28 13:16:32 +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     
KARS NM_005548.2 ?/. - c.-974G>A r.(?) p.(=)
TERF2IP NM_018975.3 ?/. - c.670+61C>T r.(=) p.(=)


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