HGVS命名之【点突变】Substitution

最近在复习HGVS命名,当做个人翻译笔记吧。

HGVS,全称是Human Genome Variation Society,人类基因组变异协会的缩写。

本周翻译的是第二部分Substitution,原文地址http://varnomen.hgvs.org/recommendations/DNA/variant/substitution/

【替换/点突变】Substitution

定义:与参考序列相比,一个核苷酸被另一个核苷酸替换

格式:前缀(所使用的参考序列)+ . +取代位置+参考核苷酸>新核苷酸,举例:g.123A>G

要点:

①接受的参考序列包括g. m. c. n.

②涉及2个及以上连续的核苷酸改变时,优先描述为缺失/插入

③经过检测,发现核苷酸未改变,描述为c.123A=,g.4567T=

④描述c.76_77delinsTT优先于c.[76A>T;77G>T],注意,依据定义,该突变不能描述为替换(类似于c.76_77AG>TT or c.76AG>TT)

⑤多态性不能描述为c.76A/G(应该描述为NM_004006.1:c.76A>G)

举例:

NC_000023.10:g.33038255C>A

a substitution of the C nucleotide at g.33038255 for an A

NG_012232.1(NM_004006.1):c.93+1G>T

a substitution of the G nucleotide at c.93+1 (coding DNA reference sequence) with a T

LRG_199t1:c.79_80delinsTT or c.[79G>T;80C>T]

the description c.79_80delinsTT is preferred over c.[79G>T;80C>T], unless either of the two variants (79G>T or c.80C>T) is known as a frequently occurring variant.

注意事项: based on the definition of a substitution, i.e. one nucleotide replaced by one other nucleotide, this change can not be described as a substitution like c.79_80GC>TT or c.79GC>TT

描述c.79_80delinsTT优先于c.[79G>T;80C>T]

NM_004006.1:c.[145C>T;147C>G]

two substitutions replacing codon CGC (position c.145 to c.147) with TGG

注意事项: the variant can also be described as NM_004006.1:c.145_147delinsTGG, i.e. a deletion/insertion. The deletion/insertion format is preferred unless either of the two variants (c.145C>T or c.147C>G) is known as a frequently occurring variant.

描述c.145_147delinsTGG优先于c.[145C>T;147C>G]

LRG_199t1:c.54G>H

a substitution of the G nucleotide at c.54 (coding DNA reference sequence) with a A, C or T (IUPAC code “H”, see Standards)

命名遵循核酸序列中“不完全指定碱基”的命名(Adenine腺嘌呤A,Cytosine胞嘧啶C,Guanine鸟嘌呤G,Thymine胸腺嘧啶T)

NM_004006.1:c.123=

a screen was performed showing that nucleotide c.123 was a “C” as in the coding DNA reference sequence (the nucleotide was not changed). Alternative NM_004006.1:c.123C=.

LRG_199t1:c.85=/T>C

a mosaic case where at position 85 besides the normal sequence (a T, described as “=”) also chromosomes are found containing a C (c.85T>C)

同源嵌合体,样本是c.85=和c.85T>C的混合体

NM_004006.1:c.85=//T>C

a chimeric case, i.e. the sample is a mix of cells containing c.85= and c.85T>C.

异源嵌合体,样本是c.85=和c.85T>C的混合体


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