Variant #0000723576 (NC_000011.9:g.64884755G>A, NM_004927.3:c.-5064G>A (MRPL49))

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.64884755G>A
DNA change (hg38) -
Published as ZNHIT2(NM_014205.4):c.371C>T (p.P124L)
ISCN -
DB-ID FAU_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) 0.00081 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAU NM_001997.4 ?/. - c.*3398C>T r.(=) p.(=)
TM7SF2 NM_003273.2 ?/. - c.*1230G>A r.(=) p.(=)
MRPL49 NM_004927.3 ?/. - c.-5064G>A r.(?) p.(=)
VPS51 NM_013265.3 ?/. - c.*5696G>A r.(=) p.(=)
ZNHIT2 NM_014205.2 ?/. - c.371C>T r.(?) p.(Pro124Leu)
SYVN1 NM_032431.2 ?/. - c.*11099C>T r.(=) p.(=)


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