Variant #0000611011 (NC_000007.13:g.16298080G>T, NM_001101426.3:c.1054C>A (ISPD))

Chromosome 7
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.16298080G>T
DNA change (hg38) g.16258455G>T
Published as CRPPA(NM_001101426.4):c.1054C>A (p.Q352K), ISPD(NM_001101426.3):c.1054C>A (p.Q352K)
ISCN -
DB-ID ISPD_000035 See all 12 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) 0.0014 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ISPD NM_001101426.3 -?/. - c.1054C>A r.(?) p.(Gln352Lys)


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