Variant #0000249132 (NC_000009.11:g.140130882A>C, NM_080877.2:c.*14A>C (SLC34A3))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140130882A>C
DNA change (hg38) g.137236430A>C
Published as SLC34A3(NM_001177317.2):c.*14A>C
ISCN -
DB-ID SLC34A3_000015 See all 2 reported entries
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) 0.38039 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM166A NM_001001710.1 -/. - c.*7270T>G r.(=) p.(=)
TUBB4B NM_006088.5 -/. - c.-4931A>C r.(?) p.(=)
SLC34A3 NM_080877.2 -/. - c.*14A>C r.(=) p.(=)


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