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HGVS命名之【点突变】Substitution

HGVS命名之【点突变】Substitution

作者: 艺语呢喃er | 来源:发表于2018-07-14 18:12 被阅读0次

    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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