Variant #0000612069 (NC_000009.11:g.26980615T>G, NM_001031689.2:c.-33572A>C (PLAA))

Chromosome 9
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.26980615T>G
DNA change (hg38) g.26980617T>G
Published as IFT74(NM_001349928.1):c.303T>G (p.L101=)
ISCN -
DB-ID IFT74_000022
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-25 12:49:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PLAA NM_001031689.2 -?/. - c.-33572A>C r.(?) p.(=)
LRRC19 NM_022901.2 -?/. - c.*14904A>C r.(=) p.(=)
IFT74 NM_025103.2 -?/. - c.303T>G r.(?) p.(Leu101=)


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