Variant #0000613103 (NC_000011.9:g.119214636G>T, NM_031433.3:c.1014C>A (MFRP))

Chromosome 11
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.119214636G>T
DNA change (hg38) g.119343926G>T
Published as C1QTNF5(NM_015645.5):c.-1623C>A, MFRP(NM_031433.3):c.1014C>A (p.S338R), MFRP(NM_031433.4):c.1014C>A (p.S338R)
ISCN -
DB-ID C1QTNF5_000011 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) 0.00101 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QTNF5 NM_001278431.1 ?/. - c.-3275C>A r.(?) p.(=)
C1QTNF5 NM_015645.3 ?/. - c.-1623C>A r.(?) p.(=)
MFRP NM_031433.3 ?/. - c.1014C>A r.(?) p.(Ser338Arg)


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