Variant #0000320577 (NC_000001.10:g.17301446G>C, NM_014675.3:c.*2505G>C (CROCC))

Chromosome 1
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.17301446G>C
DNA change (hg38) g.16974951G>C
Published as MFAP2(NM_001135247.1):c.518C>G (p.(Ala173Gly))
ISCN -
DB-ID MFAP2_000001
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) 0.00356 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MFAP2 NM_002403.3 -?/. - c.521C>G r.(?) p.(Ala174Gly)
CROCC NM_014675.3 -?/. - c.*2505G>C r.(=) p.(=)


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