Variant #0000805189 (NC_000011.9:g.562398A>C, NM_198075.3:c.*8122A>C (LRRC56))

Chromosome 11
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.562398A>C
DNA change (hg38) -
Published as RASSF7(NM_003475.4):c.444A>C (p.T148=)
ISCN -
DB-ID C11orf35_000039
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) 4.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
RASSF7 NM_003475.3 -?/. - c.444A>C r.(?) p.(Thr148=)
C11orf35 NM_173573.2 -?/. - c.-1682T>G r.(?) p.(=)
LRRC56 NM_198075.3 -?/. - c.*8122A>C r.(=) p.(=)


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