Variant #0000335590 (NC_000023.10:g.133981492A>G, NM_138819.3:c.425A>G (FAM122C))

Chromosome X
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.133981492A>G
DNA change (hg38) g.134847462A>G
Published as FAM122C(NM_001170779.1):c.345+2061A>G, FAM122C(NM_138819.3):c.425A>G (p.(Lys142Arg))
ISCN -
DB-ID FAM122C_000012 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) 6.0E-5 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 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM122C NM_138819.3 -?/. - c.425A>G r.(?) p.(Lys142Arg)


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