Variant #0000996253 (NC_000007.13:g.143080300C>G, NM_003461.4:c.908C>G (ZYX))

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.143080300C>G
DNA change (hg38) -
Published as ZYX(NM_003461.4):c.908C>G (p.(Ser303Cys))
ISCN -
DB-ID FAM131B_000006
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ZYX NM_003461.4 -?/. - c.908C>G r.(?) p.(Ser303Cys)
FAM131B NM_014690.4 -?/. - c.-21248G>C r.(?) p.(=)


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