Variant #0000692459 (NC_000017.10:g.73236133G>A, NM_015971.3:c.-21849G>A (MRPS7))

Chromosome 17
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.73236133G>A
DNA change (hg38) -
Published as GGA3(NM_001291641.1):c.1104C>T (p.G368=)
ISCN -
DB-ID NUP85_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +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     
MRPS7 NM_015971.3 -?/. - c.-21849G>A r.(?) p.(=)
NUP85 NM_024844.3 -?/. - c.*4359G>A r.(=) p.(=)
GGA3 NM_138619.2 -?/. - c.1320C>T r.(?) p.(Gly440=)


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