Variant #0001027267 (NC_000019.9:g.55341382G>C, NC_000019.9(NM_013289.2):c.1106-1G>C (KIR3DL1))

Chromosome 19
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.55341382G>C
DNA change (hg38) -
Published as KIR3DL1(NM_013289.3):c.1106-1G>C
ISCN -
DB-ID KIR2DS4_000027
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) 0.00059 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 2025-02-07 18:57:27 +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     
KIR2DS4 NM_012314.3 -?/. - c.-2838G>C r.(?) p.(=)
KIR3DL1 NM_013289.2 -?/. - c.1106-1G>C r.spl? p.?


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