Variant #0000612145 (NC_000009.11:g.4585388G>C, NM_004170.5:c.1405G>C (SLC1A1))

Chromosome 9
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.4585388G>C
DNA change (hg38) g.4585388G>C
Published as SLC1A1(NM_004170.5):c.1405G>C (p.E469Q)
ISCN -
DB-ID PPAPDC2_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) 0.00025 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPATA6L NM_001039395.3 ?/. - c.*15423C>G r.(=) p.(=)
SLC1A1 NM_004170.5 ?/. - c.1405G>C r.(?) p.(Glu469Gln)
PPAPDC2 NM_203453.3 ?/. - c.-76988G>C r.(?) p.(=)


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