Summary of mutations in RAG-deficient patients
Patient . | Gene . | Nucleotide mutation . | Effect . | Diagnosis . | Status . |
---|---|---|---|---|---|
1 | RAG-2 | G2122A | W307X | T-B-SCID | Homoz |
2 | RAG-1 | C1879G | Y589X | T-B-SCID | Homoz |
3 | RAG-1 | G2276A | E722K | T-B-SCID | Heter |
G2432T | E774X | ||||
4 | RAG-2 | ins 1665TGTTC | Frameshift | T-B-SCID | Homoz |
5 | RAG-1 | T2727A | L872X | T-B-SCID | Homoz |
6 | RAG-1 | del 2182-2189 | Frameshift | T-B-SCID | Homoz |
7 | RAG-1 | del T1173 | Frameshift | T-B-SCID | Heter |
T2727A | L872X | ||||
8 | RAG-1 | del 1521-1522 | Frameshift | T-B-SCID | Homoz |
9a | RAG-2 | G2634A | C478Y | T-B-SCID | Homoz |
10 | RAG-2 | A2622G | N474S | SCID with MFT | Homoz |
11 | RAG-1 | A2676T | N8551 | SCID with MFT | Homoz |
12 | RAG-1 | C2801T | R897X | SCID with MFT | Heter |
G1983A | R624H | ||||
13 | RAG-1 | G2988A | W959X | SCID with MFT | Homoz |
9b | RAG-2 | G2634A | C478Y | SCID with MFT | Homoz |
14 | RAG-1 | T2926G | Y938X | SCID with MFT | Homoz |
15 | RAG-1 | Del 1258 | Frameshift | SCID with MFT | Homoz |
16a | RAG-1 | C1298T | R396C | Atypical SCID/OS | Homoz |
17 | RAG-1 | G1533A | R474H | Atypical SCID/OS | Heter |
A2370T | H753L | ||||
18 | RAG-1 | G1409A | V433M | Atypical SCID/OS | Heter |
C1443T | A444V | ||||
19 | RAG-1 | C1631T | R507W | Atypical SCID/OS | Heter |
C1793T | R561C | ||||
20 | RAG-2 | G1887A | R229Q | Atypical SCID/OS | Heter |
Locus deletion | |||||
21 | RAG-1 | A1398G | D429G | Atypical SCID/OS | Heter |
del 368-369 | Frameshift | ||||
22 | RAG-1 | C2633T | R841W | Atypical SCID/OS | Heter |
G1341A | R410Q | ||||
23 | RAG-1 | C1443T | A444V | Atypical SCID/OS | Homoz |
24 | RAG-2 | C1886T | R229W | Atypical SCID/OS | Homoz |
25 | RAG-1 | G1678T | W522C | Atypical SCID/OS | Heter |
G2276A | E722K | ||||
26 | RAG-2 | G1887A | R229Q | Atypical SCID/OS | Homoz |
27 | RAG-1 | T1313C | S401P | Omenn | Homoz |
28 | RAG-1 | G1095A | C328Y | Omenn | Homoz |
29 | RAG-2 | T1818G | F206C | Omenn | Heter |
C1643T | R148X | ||||
30a | RAG-2 | C1886T | R229W | Omenn | Homoz |
30b | RAG-2 | C1886T | R229W | Omenn | Homoz |
31 | RAG-1 | G1299A | R396H | Omenn | Heter |
del 1723-1735 | Frameshift | ||||
32 | RAG-1 | A2118G | E669G | Omenn | Heter |
C2812A | C900X | ||||
33 | RAG-1 | C1298T | R396C | Omenn | Heter |
A2847G | Y912C | ||||
34 | RAG-2 | C1324G | C41W | Omenn | Heter |
T2055G | M285R | ||||
35 | RAG-1 | G1794A | R561H | Omenn | Homoz |
36 | RAG-1 | G1299T | R396L | Omenn | Heter |
G3036A | R975Q | ||||
16b | RAG-1 | C1298T | R396C | Omenn | Homoz |
37 | RAG-1 | C1793T | R561C | Omenn | Heter |
G2322A | R737H | ||||
38 | RAG-1 | del 368-369 | Frameshift | Omenn | Heter |
G2276A | E722K | ||||
39 | RAG-1 | del 368-369 | Frameshift | Omenn | Heter |
RAG-1 | C1982T | R624C | |||
40 | RAG-1 | G1789T | R559S | Omenn | Heter |
A1415G | M435V | ||||
41 | RAG-1 | C1443T | A444V | Omenn | Homoz |
Patient . | Gene . | Nucleotide mutation . | Effect . | Diagnosis . | Status . |
---|---|---|---|---|---|
1 | RAG-2 | G2122A | W307X | T-B-SCID | Homoz |
2 | RAG-1 | C1879G | Y589X | T-B-SCID | Homoz |
3 | RAG-1 | G2276A | E722K | T-B-SCID | Heter |
G2432T | E774X | ||||
4 | RAG-2 | ins 1665TGTTC | Frameshift | T-B-SCID | Homoz |
5 | RAG-1 | T2727A | L872X | T-B-SCID | Homoz |
6 | RAG-1 | del 2182-2189 | Frameshift | T-B-SCID | Homoz |
7 | RAG-1 | del T1173 | Frameshift | T-B-SCID | Heter |
T2727A | L872X | ||||
8 | RAG-1 | del 1521-1522 | Frameshift | T-B-SCID | Homoz |
9a | RAG-2 | G2634A | C478Y | T-B-SCID | Homoz |
10 | RAG-2 | A2622G | N474S | SCID with MFT | Homoz |
11 | RAG-1 | A2676T | N8551 | SCID with MFT | Homoz |
12 | RAG-1 | C2801T | R897X | SCID with MFT | Heter |
G1983A | R624H | ||||
13 | RAG-1 | G2988A | W959X | SCID with MFT | Homoz |
9b | RAG-2 | G2634A | C478Y | SCID with MFT | Homoz |
14 | RAG-1 | T2926G | Y938X | SCID with MFT | Homoz |
15 | RAG-1 | Del 1258 | Frameshift | SCID with MFT | Homoz |
16a | RAG-1 | C1298T | R396C | Atypical SCID/OS | Homoz |
17 | RAG-1 | G1533A | R474H | Atypical SCID/OS | Heter |
A2370T | H753L | ||||
18 | RAG-1 | G1409A | V433M | Atypical SCID/OS | Heter |
C1443T | A444V | ||||
19 | RAG-1 | C1631T | R507W | Atypical SCID/OS | Heter |
C1793T | R561C | ||||
20 | RAG-2 | G1887A | R229Q | Atypical SCID/OS | Heter |
Locus deletion | |||||
21 | RAG-1 | A1398G | D429G | Atypical SCID/OS | Heter |
del 368-369 | Frameshift | ||||
22 | RAG-1 | C2633T | R841W | Atypical SCID/OS | Heter |
G1341A | R410Q | ||||
23 | RAG-1 | C1443T | A444V | Atypical SCID/OS | Homoz |
24 | RAG-2 | C1886T | R229W | Atypical SCID/OS | Homoz |
25 | RAG-1 | G1678T | W522C | Atypical SCID/OS | Heter |
G2276A | E722K | ||||
26 | RAG-2 | G1887A | R229Q | Atypical SCID/OS | Homoz |
27 | RAG-1 | T1313C | S401P | Omenn | Homoz |
28 | RAG-1 | G1095A | C328Y | Omenn | Homoz |
29 | RAG-2 | T1818G | F206C | Omenn | Heter |
C1643T | R148X | ||||
30a | RAG-2 | C1886T | R229W | Omenn | Homoz |
30b | RAG-2 | C1886T | R229W | Omenn | Homoz |
31 | RAG-1 | G1299A | R396H | Omenn | Heter |
del 1723-1735 | Frameshift | ||||
32 | RAG-1 | A2118G | E669G | Omenn | Heter |
C2812A | C900X | ||||
33 | RAG-1 | C1298T | R396C | Omenn | Heter |
A2847G | Y912C | ||||
34 | RAG-2 | C1324G | C41W | Omenn | Heter |
T2055G | M285R | ||||
35 | RAG-1 | G1794A | R561H | Omenn | Homoz |
36 | RAG-1 | G1299T | R396L | Omenn | Heter |
G3036A | R975Q | ||||
16b | RAG-1 | C1298T | R396C | Omenn | Homoz |
37 | RAG-1 | C1793T | R561C | Omenn | Heter |
G2322A | R737H | ||||
38 | RAG-1 | del 368-369 | Frameshift | Omenn | Heter |
G2276A | E722K | ||||
39 | RAG-1 | del 368-369 | Frameshift | Omenn | Heter |
RAG-1 | C1982T | R624C | |||
40 | RAG-1 | G1789T | R559S | Omenn | Heter |
A1415G | M435V | ||||
41 | RAG-1 | C1443T | A444V | Omenn | Homoz |