Variant #0000723266 (NC_000011.9:g.119213688G>C, NM_031433.3:c.1150C>G (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.119213688G>C
DNA change (hg38) -
Published as MFRP(NM_031433.3):c.1150C>G (p.H384D)
ISCN -
DB-ID C1QTNF5_000055
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) 1.0E-5 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 2021-02-08 18:36:18 +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.-2327C>G r.(?) p.(=)
C1QTNF5 NM_015645.3 ?/. - c.-1487C>G r.(?) p.(=)
MFRP NM_031433.3 ?/. - c.1150C>G r.(?) p.(His384Asp)


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