T961C T961 rs3888511 |
rCRS Ref: T. Yoruba (hg18) Position: 963. This mutation results in a repeating sequence of 10 C alleles starting from hg38:956. Also see branches: U1a1a7, U5a1c2a2, A5b, B2i1, D4h2, H10e3a, H3r, H5a1f, L0a1b1a1, L6, M2a1a2a1a, M44, M7a2a2, N9a2, U4a1a, U5a1c2, A2u2a, A2g93, A2d7, A2c3, H8b1w, A2ac89. See also T961A.
NIH DBSNP b153 GRCh38p12 ClinVar? Position hg18: 963
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RSRS
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T |
C |
M |
961 |
961 |