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Variant (rsID / SNP)

rs11101677

TUBGCP2

rs11101677 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TUBGCP2. Location: chromosome 10, position 135,094,925. The table records no clinical significance for this variant.

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Reference-table entries

TUBGCP2Not classified
Variant type
missense_variant
Chromosome / position
10:135094925
HGVS
NM_001256617.2,c.2509G>A,p.Ala837Thr
Allele change
Missense_A809T

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.